Canonical Allele Identifier: CA1208363279

Gene: RABGAP1L

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.174892127_174892130delinsTGGC , CM000663.2:g.174892127_174892130delinsTGGC	GRCh38
NC_000001.10:g.174861264_174861267delinsTGGC , CM000663.1:g.174861264_174861267delinsTGGC	GRCh37
NC_000001.9:g.173127887_173127890delinsTGGC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681986.1:c.2341-65330_2341-65327delinsTGGC MANE Select	ENSP00000507884.1:n.2341-65330_2341-65327delinsTGGC
ENST00000251507.8:c.2341-65330_2341-65327delinsTGGC	ENSP00000251507.4:n.2341-65330_2341-65327delinsTGGC
ENST00000325589.9:c.262-65330_262-65327delinsTGGC	ENSP00000318603.5:n.262-65330_262-65327delinsTGGC
ENST00000347255.6:c.322-65330_322-65327delinsTGGC	ENSP00000281844.5:n.322-65330_322-65327delinsTGGC
ENST00000367686.7:c.*181+14522_*181+14525delinsTGGC	ENSP00000489178.1:n.*181+14522_*181+14525delinsTGGC
ENST00000367687.5:c.319-65330_319-65327delinsTGGC	ENSP00000356660.1:n.319-65330_319-65327delinsTGGC
ENST00000392064.6:c.111+14522_111+14525delinsTGGC	ENSP00000375916.2:n.111+14522_111+14525delinsTGGC
ENST00000465412.5:c.111+14522_111+14525delinsTGGC	ENSP00000435911.1:n.111+14522_111+14525delinsTGGC
ENST00000469553.6:c.*181+14522_*181+14525delinsTGGC	ENSP00000432734.1:n.*181+14522_*181+14525delinsTGGC
ENST00000478442.5:c.111+14522_111+14525delinsTGGC	ENSP00000434600.1:n.111+14522_111+14525delinsTGGC
ENST00000486220.5:c.111+14522_111+14525delinsTGGC	ENSP00000432490.1:n.111+14522_111+14525delinsTGGC
ENST00000489615.5:c.298-65330_298-65327delinsTGGC	ENSP00000420660.1:n.298-65330_298-65327delinsTGGC
ENST00000529145.6:c.262-65330_262-65327delinsTGGC	ENSP00000489163.1:n.262-65330_262-65327delinsTGGC
NM_001035230.2:c.111+14522_111+14525delinsTGGC	NP_001030307.1:n.111+14522_111+14525delinsTGGC
NM_001243763.1:c.111+14522_111+14525delinsTGGC	NP_001230692.1:n.111+14522_111+14525delinsTGGC
NM_001243765.1:c.298-65330_298-65327delinsTGGC	NP_001230694.1:n.298-65330_298-65327delinsTGGC
NM_014857.4:c.2341-65330_2341-65327delinsTGGC	NP_055672.3:n.2341-65330_2341-65327delinsTGGC
XM_005245680.1:c.2341-65330_2341-65327delinsTGGC	XP_005245737.1:n.2341-65330_2341-65327delinsTGGC
XM_005245681.1:c.2230-65330_2230-65327delinsTGGC	XP_005245738.1:n.2230-65330_2230-65327delinsTGGC
XM_006711693.1:c.2341-65330_2341-65327delinsTGGC	XP_006711756.1:n.2341-65330_2341-65327delinsTGGC
XM_011510223.1:c.2341-65330_2341-65327delinsTGGC	XP_011508525.1:n.2341-65330_2341-65327delinsTGGC
XR_922003.1:n.2761+14522_2761+14525delinsTGGC
XR_922004.1:n.2761+14522_2761+14525delinsTGGC
NM_001330989.1:c.111+14522_111+14525delinsTGGC	NP_001317918.1:n.111+14522_111+14525delinsTGGC
NM_001366446.1:c.2341-65330_2341-65327delinsTGGC MANE Select	NP_001353375.1:n.2341-65330_2341-65327delinsTGGC
NM_001366447.1:c.2230-65330_2230-65327delinsTGGC	NP_001353376.1:n.2230-65330_2230-65327delinsTGGC
NM_001366448.1:c.2341-65330_2341-65327delinsTGGC	NP_001353377.1:n.2341-65330_2341-65327delinsTGGC
NM_001366450.1:c.262-65330_262-65327delinsTGGC	NP_001353379.1:n.262-65330_262-65327delinsTGGC
NM_001366451.1:c.-329+14522_-329+14525delinsTGGC	NP_001353380.1:n.-329+14522_-329+14525delinsTGGC
NM_001366452.1:c.322-65330_322-65327delinsTGGC	NP_001353381.1:n.322-65330_322-65327delinsTGGC
NM_001366453.1:c.319-65330_319-65327delinsTGGC	NP_001353382.1:n.319-65330_319-65327delinsTGGC
NM_001366454.1:c.111+14522_111+14525delinsTGGC	NP_001353383.1:n.111+14522_111+14525delinsTGGC
NM_001366455.1:c.298-65330_298-65327delinsTGGC	NP_001353384.1:n.298-65330_298-65327delinsTGGC
NM_001366456.1:c.298-65330_298-65327delinsTGGC	NP_001353385.1:n.298-65330_298-65327delinsTGGC
NM_001366457.1:c.-46+17621_-46+17624delinsTGGC	NP_001353386.1:n.-46+17621_-46+17624delinsTGGC
NR_158982.1:n.2725+14522_2725+14525delinsTGGC
XM_005245681.2:c.2230-65330_2230-65327delinsTGGC	XP_005245738.1:n.2230-65330_2230-65327delinsTGGC
XM_011510223.2:c.2341-65330_2341-65327delinsTGGC	XP_011508525.1:n.2341-65330_2341-65327delinsTGGC
XM_017002996.1:c.111+14522_111+14525delinsTGGC	XP_016858485.1:n.111+14522_111+14525delinsTGGC
XM_017002997.1:c.111+14522_111+14525delinsTGGC	XP_016858486.1:n.111+14522_111+14525delinsTGGC
XM_024451295.1:c.111+14522_111+14525delinsTGGC	XP_024307063.1:n.111+14522_111+14525delinsTGGC
NM_001243765.2:c.298-65330_298-65327delinsTGGC	NP_001230694.1:n.298-65330_298-65327delinsTGGC
NM_001330989.2:c.111+14522_111+14525delinsTGGC	NP_001317918.1:n.111+14522_111+14525delinsTGGC
NM_001035230.3:c.111+14522_111+14525delinsTGGC	NP_001030307.1:n.111+14522_111+14525delinsTGGC
NM_001243763.2:c.111+14522_111+14525delinsTGGC	NP_001230692.1:n.111+14522_111+14525delinsTGGC
NM_014857.5:c.2341-65330_2341-65327delinsTGGC	NP_055672.3:n.2341-65330_2341-65327delinsTGGC