Canonical Allele Identifier: CA10851219
Gene: RABGAP1L HGNC NCBI

Linked Data

dbSNP Id: rs12078839

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.174892350C>G , CM000663.2:g.174892350C>G GRCh38
NC_000001.10:g.174861487C>G , CM000663.1:g.174861487C>G GRCh37
NC_000001.9:g.173128110C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000681986.1:c.2341-65107C>G MANE Select ENSP00000507884.1:n.2341-65107C>G
ENST00000251507.8:c.2341-65107C>G ENSP00000251507.4:n.2341-65107C>G
ENST00000325589.9:c.262-65107C>G ENSP00000318603.5:n.262-65107C>G
ENST00000347255.6:c.322-65107C>G ENSP00000281844.5:n.322-65107C>G
ENST00000367686.7:c.*181+14745C>G ENSP00000489178.1:n.*181+14745C>G
ENST00000367687.5:c.319-65107C>G ENSP00000356660.1:n.319-65107C>G
ENST00000392064.6:c.111+14745C>G ENSP00000375916.2:n.111+14745C>G
ENST00000465412.5:c.111+14745C>G ENSP00000435911.1:n.111+14745C>G
ENST00000469553.6:c.*181+14745C>G ENSP00000432734.1:n.*181+14745C>G
ENST00000478442.5:c.111+14745C>G ENSP00000434600.1:n.111+14745C>G
ENST00000486220.5:c.111+14745C>G ENSP00000432490.1:n.111+14745C>G
ENST00000489615.5:c.298-65107C>G ENSP00000420660.1:n.298-65107C>G
ENST00000529145.6:c.262-65107C>G ENSP00000489163.1:n.262-65107C>G
NM_001035230.2:c.111+14745C>G NP_001030307.1:n.111+14745C>G
NM_001243763.1:c.111+14745C>G NP_001230692.1:n.111+14745C>G
NM_001243765.1:c.298-65107C>G NP_001230694.1:n.298-65107C>G
NM_014857.4:c.2341-65107C>G NP_055672.3:n.2341-65107C>G
XM_005245680.1:c.2341-65107C>G XP_005245737.1:n.2341-65107C>G
XM_005245681.1:c.2230-65107C>G XP_005245738.1:n.2230-65107C>G
XM_006711693.1:c.2341-65107C>G XP_006711756.1:n.2341-65107C>G
XM_011510223.1:c.2341-65107C>G XP_011508525.1:n.2341-65107C>G
XR_922003.1:n.2761+14745C>G
XR_922004.1:n.2761+14745C>G
NM_001330989.1:c.111+14745C>G NP_001317918.1:n.111+14745C>G
NM_001366446.1:c.2341-65107C>G MANE Select NP_001353375.1:n.2341-65107C>G
NM_001366447.1:c.2230-65107C>G NP_001353376.1:n.2230-65107C>G
NM_001366448.1:c.2341-65107C>G NP_001353377.1:n.2341-65107C>G
NM_001366450.1:c.262-65107C>G NP_001353379.1:n.262-65107C>G
NM_001366451.1:c.-329+14745C>G NP_001353380.1:n.-329+14745C>G
NM_001366452.1:c.322-65107C>G NP_001353381.1:n.322-65107C>G
NM_001366453.1:c.319-65107C>G NP_001353382.1:n.319-65107C>G
NM_001366454.1:c.111+14745C>G NP_001353383.1:n.111+14745C>G
NM_001366455.1:c.298-65107C>G NP_001353384.1:n.298-65107C>G
NM_001366456.1:c.298-65107C>G NP_001353385.1:n.298-65107C>G
NM_001366457.1:c.-46+17844C>G NP_001353386.1:n.-46+17844C>G
NR_158982.1:n.2725+14745C>G
XM_005245681.2:c.2230-65107C>G XP_005245738.1:n.2230-65107C>G
XM_011510223.2:c.2341-65107C>G XP_011508525.1:n.2341-65107C>G
XM_017002996.1:c.111+14745C>G XP_016858485.1:n.111+14745C>G
XM_017002997.1:c.111+14745C>G XP_016858486.1:n.111+14745C>G
XM_024451295.1:c.111+14745C>G XP_024307063.1:n.111+14745C>G
NM_001243765.2:c.298-65107C>G NP_001230694.1:n.298-65107C>G
NM_001330989.2:c.111+14745C>G NP_001317918.1:n.111+14745C>G
NM_001035230.3:c.111+14745C>G NP_001030307.1:n.111+14745C>G
NM_001243763.2:c.111+14745C>G NP_001230692.1:n.111+14745C>G
NM_014857.5:c.2341-65107C>G NP_055672.3:n.2341-65107C>G