Canonical Allele Identifier: CA1009361128
Gene: RABGAP1L HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.174892731_174892732insTTTTTTTTTTTTTTTTTTTT , CM000663.2:g.174892731_174892732insTTTTTTTTTTTTTTTTTTTT GRCh38
NC_000001.10:g.174861868_174861869insTTTTTTTTTTTTTTTTTTTT , CM000663.1:g.174861868_174861869insTTTTTTTTTTTTTTTTTTTT GRCh37
NC_000001.9:g.173128491_173128492insTTTTTTTTTTTTTTTTTTTT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000681986.1:c.2341-64726_2341-64725insTTTTTTTTTTTTTTTTTTTT MANE Select ENSP00000507884.1:n.2341-64726_2341-64725insTTTTTTTTTTTTTTTTT...
ENST00000251507.8:c.2341-64726_2341-64725insTTTTTTTTTTTTTTTTTTTT ENSP00000251507.4:n.2341-64726_2341-64725insTTTTTTTTTTTTTTTTT...
ENST00000325589.9:c.262-64726_262-64725insTTTTTTTTTTTTTTTTTTTT ENSP00000318603.5:n.262-64726_262-64725insTTTTTTTTTTTTTTTTTTT...
ENST00000347255.6:c.322-64726_322-64725insTTTTTTTTTTTTTTTTTTTT ENSP00000281844.5:n.322-64726_322-64725insTTTTTTTTTTTTTTTTTTT...
ENST00000367686.7:c.*181+15126_*181+15127insTTTTTTTTTTTTTTTTTTTT ENSP00000489178.1:n.*181+15126_*181+15127insTTTTTTTTTTTTTTTTT...
ENST00000367687.5:c.319-64726_319-64725insTTTTTTTTTTTTTTTTTTTT ENSP00000356660.1:n.319-64726_319-64725insTTTTTTTTTTTTTTTTTTT...
ENST00000392064.6:c.111+15126_111+15127insTTTTTTTTTTTTTTTTTTTT ENSP00000375916.2:n.111+15126_111+15127insTTTTTTTTTTTTTTTTTTT...
ENST00000448158.1:n.286+29_286+30insTTTTTTTTTTTTTTTTTTTT
ENST00000465412.5:c.111+15126_111+15127insTTTTTTTTTTTTTTTTTTTT ENSP00000435911.1:n.111+15126_111+15127insTTTTTTTTTTTTTTTTTTT...
ENST00000469553.6:c.*181+15126_*181+15127insTTTTTTTTTTTTTTTTTTTT ENSP00000432734.1:n.*181+15126_*181+15127insTTTTTTTTTTTTTTTTT...
ENST00000478442.5:c.111+15126_111+15127insTTTTTTTTTTTTTTTTTTTT ENSP00000434600.1:n.111+15126_111+15127insTTTTTTTTTTTTTTTTTTT...
ENST00000486220.5:c.111+15126_111+15127insTTTTTTTTTTTTTTTTTTTT ENSP00000432490.1:n.111+15126_111+15127insTTTTTTTTTTTTTTTTTTT...
ENST00000489615.5:c.298-64726_298-64725insTTTTTTTTTTTTTTTTTTTT ENSP00000420660.1:n.298-64726_298-64725insTTTTTTTTTTTTTTTTTTT...
ENST00000529145.6:c.262-64726_262-64725insTTTTTTTTTTTTTTTTTTTT ENSP00000489163.1:n.262-64726_262-64725insTTTTTTTTTTTTTTTTTTT...
NM_001035230.2:c.111+15126_111+15127insTTTTTTTTTTTTTTTTTTTT NP_001030307.1:n.111+15126_111+15127insTTTTTTTTTTTTTTTTTTTT
NM_001243763.1:c.111+15126_111+15127insTTTTTTTTTTTTTTTTTTTT NP_001230692.1:n.111+15126_111+15127insTTTTTTTTTTTTTTTTTTTT
NM_001243765.1:c.298-64726_298-64725insTTTTTTTTTTTTTTTTTTTT NP_001230694.1:n.298-64726_298-64725insTTTTTTTTTTTTTTTTTTTT
NM_014857.4:c.2341-64726_2341-64725insTTTTTTTTTTTTTTTTTTTT NP_055672.3:n.2341-64726_2341-64725insTTTTTTTTTTTTTTTTTTTT
XM_005245680.1:c.2341-64726_2341-64725insTTTTTTTTTTTTTTTTTTTT XP_005245737.1:n.2341-64726_2341-64725insTTTTTTTTTTTTTTTTTTTT...
XM_005245681.1:c.2230-64726_2230-64725insTTTTTTTTTTTTTTTTTTTT XP_005245738.1:n.2230-64726_2230-64725insTTTTTTTTTTTTTTTTTTTT...
XM_006711693.1:c.2341-64726_2341-64725insTTTTTTTTTTTTTTTTTTTT XP_006711756.1:n.2341-64726_2341-64725insTTTTTTTTTTTTTTTTTTTT...
XM_011510223.1:c.2341-64726_2341-64725insTTTTTTTTTTTTTTTTTTTT XP_011508525.1:n.2341-64726_2341-64725insTTTTTTTTTTTTTTTTTTTT...
XR_922003.1:n.2761+15126_2761+15127insTTTTTTTTTTTTTTTTTTTT
XR_922004.1:n.2761+15126_2761+15127insTTTTTTTTTTTTTTTTTTTT
NM_001330989.1:c.111+15126_111+15127insTTTTTTTTTTTTTTTTTTTT NP_001317918.1:n.111+15126_111+15127insTTTTTTTTTTTTTTTTTTTT
NM_001366446.1:c.2341-64726_2341-64725insTTTTTTTTTTTTTTTTTTTT MANE Select NP_001353375.1:n.2341-64726_2341-64725insTTTTTTTTTTTTTTTTTTTT...
NM_001366447.1:c.2230-64726_2230-64725insTTTTTTTTTTTTTTTTTTTT NP_001353376.1:n.2230-64726_2230-64725insTTTTTTTTTTTTTTTTTTTT...
NM_001366448.1:c.2341-64726_2341-64725insTTTTTTTTTTTTTTTTTTTT NP_001353377.1:n.2341-64726_2341-64725insTTTTTTTTTTTTTTTTTTTT...
NM_001366450.1:c.262-64726_262-64725insTTTTTTTTTTTTTTTTTTTT NP_001353379.1:n.262-64726_262-64725insTTTTTTTTTTTTTTTTTTTT
NM_001366451.1:c.-329+15126_-329+15127insTTTTTTTTTTTTTTTTTTTT NP_001353380.1:n.-329+15126_-329+15127insTTTTTTTTTTTTTTTTTTTT...
NM_001366452.1:c.322-64726_322-64725insTTTTTTTTTTTTTTTTTTTT NP_001353381.1:n.322-64726_322-64725insTTTTTTTTTTTTTTTTTTTT
NM_001366453.1:c.319-64726_319-64725insTTTTTTTTTTTTTTTTTTTT NP_001353382.1:n.319-64726_319-64725insTTTTTTTTTTTTTTTTTTTT
NM_001366454.1:c.111+15126_111+15127insTTTTTTTTTTTTTTTTTTTT NP_001353383.1:n.111+15126_111+15127insTTTTTTTTTTTTTTTTTTTT
NM_001366455.1:c.298-64726_298-64725insTTTTTTTTTTTTTTTTTTTT NP_001353384.1:n.298-64726_298-64725insTTTTTTTTTTTTTTTTTTTT
NM_001366456.1:c.298-64726_298-64725insTTTTTTTTTTTTTTTTTTTT NP_001353385.1:n.298-64726_298-64725insTTTTTTTTTTTTTTTTTTTT
NM_001366457.1:c.-46+18225_-46+18226insTTTTTTTTTTTTTTTTTTTT NP_001353386.1:n.-46+18225_-46+18226insTTTTTTTTTTTTTTTTTTTT
NR_158982.1:n.2725+15126_2725+15127insTTTTTTTTTTTTTTTTTTTT
XM_005245681.2:c.2230-64726_2230-64725insTTTTTTTTTTTTTTTTTTTT XP_005245738.1:n.2230-64726_2230-64725insTTTTTTTTTTTTTTTTTTTT...
XM_011510223.2:c.2341-64726_2341-64725insTTTTTTTTTTTTTTTTTTTT XP_011508525.1:n.2341-64726_2341-64725insTTTTTTTTTTTTTTTTTTTT...
XM_017002996.1:c.111+15126_111+15127insTTTTTTTTTTTTTTTTTTTT XP_016858485.1:n.111+15126_111+15127insTTTTTTTTTTTTTTTTTTTT
XM_017002997.1:c.111+15126_111+15127insTTTTTTTTTTTTTTTTTTTT XP_016858486.1:n.111+15126_111+15127insTTTTTTTTTTTTTTTTTTTT
XM_024451295.1:c.111+15126_111+15127insTTTTTTTTTTTTTTTTTTTT XP_024307063.1:n.111+15126_111+15127insTTTTTTTTTTTTTTTTTTTT
NM_001243765.2:c.298-64726_298-64725insTTTTTTTTTTTTTTTTTTTT NP_001230694.1:n.298-64726_298-64725insTTTTTTTTTTTTTTTTTTTT
NM_001330989.2:c.111+15126_111+15127insTTTTTTTTTTTTTTTTTTTT NP_001317918.1:n.111+15126_111+15127insTTTTTTTTTTTTTTTTTTTT
NM_001035230.3:c.111+15126_111+15127insTTTTTTTTTTTTTTTTTTTT NP_001030307.1:n.111+15126_111+15127insTTTTTTTTTTTTTTTTTTTT
NM_001243763.2:c.111+15126_111+15127insTTTTTTTTTTTTTTTTTTTT NP_001230692.1:n.111+15126_111+15127insTTTTTTTTTTTTTTTTTTTT
NM_014857.5:c.2341-64726_2341-64725insTTTTTTTTTTTTTTTTTTTT NP_055672.3:n.2341-64726_2341-64725insTTTTTTTTTTTTTTTTTTTT