Canonical Allele Identifier: CA2649191644

Gene: RABGAP1L

Linked Data

• gnomAD v4: 1-174892727-T-TA

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.174892727_174892728insA , CM000663.2:g.174892727_174892728insA	GRCh38
NC_000001.10:g.174861864_174861865insA , CM000663.1:g.174861864_174861865insA	GRCh37
NC_000001.9:g.173128487_173128488insA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681986.1:c.2341-64730_2341-64729insA MANE Select	ENSP00000507884.1:n.2341-64730_2341-64729insA
ENST00000251507.8:c.2341-64730_2341-64729insA	ENSP00000251507.4:n.2341-64730_2341-64729insA
ENST00000325589.9:c.262-64730_262-64729insA	ENSP00000318603.5:n.262-64730_262-64729insA
ENST00000347255.6:c.322-64730_322-64729insA	ENSP00000281844.5:n.322-64730_322-64729insA
ENST00000367686.7:c.*181+15122_*181+15123insA	ENSP00000489178.1:n.*181+15122_*181+15123insA
ENST00000367687.5:c.319-64730_319-64729insA	ENSP00000356660.1:n.319-64730_319-64729insA
ENST00000392064.6:c.111+15122_111+15123insA	ENSP00000375916.2:n.111+15122_111+15123insA
ENST00000448158.1:n.286+25_286+26insA
ENST00000465412.5:c.111+15122_111+15123insA	ENSP00000435911.1:n.111+15122_111+15123insA
ENST00000469553.6:c.*181+15122_*181+15123insA	ENSP00000432734.1:n.*181+15122_*181+15123insA
ENST00000478442.5:c.111+15122_111+15123insA	ENSP00000434600.1:n.111+15122_111+15123insA
ENST00000486220.5:c.111+15122_111+15123insA	ENSP00000432490.1:n.111+15122_111+15123insA
ENST00000489615.5:c.298-64730_298-64729insA	ENSP00000420660.1:n.298-64730_298-64729insA
ENST00000529145.6:c.262-64730_262-64729insA	ENSP00000489163.1:n.262-64730_262-64729insA
NM_001035230.2:c.111+15122_111+15123insA	NP_001030307.1:n.111+15122_111+15123insA
NM_001243763.1:c.111+15122_111+15123insA	NP_001230692.1:n.111+15122_111+15123insA
NM_001243765.1:c.298-64730_298-64729insA	NP_001230694.1:n.298-64730_298-64729insA
NM_014857.4:c.2341-64730_2341-64729insA	NP_055672.3:n.2341-64730_2341-64729insA
XM_005245680.1:c.2341-64730_2341-64729insA	XP_005245737.1:n.2341-64730_2341-64729insA
XM_005245681.1:c.2230-64730_2230-64729insA	XP_005245738.1:n.2230-64730_2230-64729insA
XM_006711693.1:c.2341-64730_2341-64729insA	XP_006711756.1:n.2341-64730_2341-64729insA
XM_011510223.1:c.2341-64730_2341-64729insA	XP_011508525.1:n.2341-64730_2341-64729insA
XR_922003.1:n.2761+15122_2761+15123insA
XR_922004.1:n.2761+15122_2761+15123insA
NM_001330989.1:c.111+15122_111+15123insA	NP_001317918.1:n.111+15122_111+15123insA
NM_001366446.1:c.2341-64730_2341-64729insA MANE Select	NP_001353375.1:n.2341-64730_2341-64729insA
NM_001366447.1:c.2230-64730_2230-64729insA	NP_001353376.1:n.2230-64730_2230-64729insA
NM_001366448.1:c.2341-64730_2341-64729insA	NP_001353377.1:n.2341-64730_2341-64729insA
NM_001366450.1:c.262-64730_262-64729insA	NP_001353379.1:n.262-64730_262-64729insA
NM_001366451.1:c.-329+15122_-329+15123insA	NP_001353380.1:n.-329+15122_-329+15123insA
NM_001366452.1:c.322-64730_322-64729insA	NP_001353381.1:n.322-64730_322-64729insA
NM_001366453.1:c.319-64730_319-64729insA	NP_001353382.1:n.319-64730_319-64729insA
NM_001366454.1:c.111+15122_111+15123insA	NP_001353383.1:n.111+15122_111+15123insA
NM_001366455.1:c.298-64730_298-64729insA	NP_001353384.1:n.298-64730_298-64729insA
NM_001366456.1:c.298-64730_298-64729insA	NP_001353385.1:n.298-64730_298-64729insA
NM_001366457.1:c.-46+18221_-46+18222insA	NP_001353386.1:n.-46+18221_-46+18222insA
NR_158982.1:n.2725+15122_2725+15123insA
XM_005245681.2:c.2230-64730_2230-64729insA	XP_005245738.1:n.2230-64730_2230-64729insA
XM_011510223.2:c.2341-64730_2341-64729insA	XP_011508525.1:n.2341-64730_2341-64729insA
XM_017002996.1:c.111+15122_111+15123insA	XP_016858485.1:n.111+15122_111+15123insA
XM_017002997.1:c.111+15122_111+15123insA	XP_016858486.1:n.111+15122_111+15123insA
XM_024451295.1:c.111+15122_111+15123insA	XP_024307063.1:n.111+15122_111+15123insA
NM_001243765.2:c.298-64730_298-64729insA	NP_001230694.1:n.298-64730_298-64729insA
NM_001330989.2:c.111+15122_111+15123insA	NP_001317918.1:n.111+15122_111+15123insA
NM_001035230.3:c.111+15122_111+15123insA	NP_001030307.1:n.111+15122_111+15123insA
NM_001243763.2:c.111+15122_111+15123insA	NP_001230692.1:n.111+15122_111+15123insA
NM_014857.5:c.2341-64730_2341-64729insA	NP_055672.3:n.2341-64730_2341-64729insA