Canonical Allele Identifier: CA1208109268

Gene: RABGAP1L

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.174323011_174323013delinsTGA , CM000663.2:g.174323011_174323013delinsTGA	GRCh38
NC_000001.10:g.174292149_174292151delinsTGA , CM000663.1:g.174292149_174292151delinsTGA	GRCh37
NC_000001.9:g.172558772_172558774delinsTGA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681986.1:c.1465+17884_1465+17886delinsTGA MANE Select	ENSP00000507884.1:n.1465+17884_1465+17886delinsTGA
ENST00000251507.8:c.1465+17884_1465+17886delinsTGA	ENSP00000251507.4:n.1465+17884_1465+17886delinsTGA
ENST00000357444.10:c.1354+17884_1354+17886delinsTGA	ENSP00000350027.6:n.1354+17884_1354+17886delinsTGA
ENST00000367690.5:c.406+17884_406+17886delinsTGA	ENSP00000489605.1:n.406+17884_406+17886delinsTGA
ENST00000457696.1:c.1501+17884_1501+17886delinsTGA	ENSP00000403136.1:n.1501+17884_1501+17886delinsTGA
NM_014857.4:c.1465+17884_1465+17886delinsTGA	NP_055672.3:n.1465+17884_1465+17886delinsTGA
XM_005245680.1:c.1465+17884_1465+17886delinsTGA	XP_005245737.1:n.1465+17884_1465+17886delinsTGA
XM_005245681.1:c.1354+17884_1354+17886delinsTGA	XP_005245738.1:n.1354+17884_1354+17886delinsTGA
XM_006711693.1:c.1465+17884_1465+17886delinsTGA	XP_006711756.1:n.1465+17884_1465+17886delinsTGA
XM_011510223.1:c.1465+17884_1465+17886delinsTGA	XP_011508525.1:n.1465+17884_1465+17886delinsTGA
XR_922003.1:n.1672+17884_1672+17886delinsTGA
XR_922004.1:n.1672+17884_1672+17886delinsTGA
NM_001366445.1:c.1354+17884_1354+17886delinsTGA	NP_001353374.1:n.1354+17884_1354+17886delinsTGA
NM_001366446.1:c.1465+17884_1465+17886delinsTGA MANE Select	NP_001353375.1:n.1465+17884_1465+17886delinsTGA
NM_001366447.1:c.1354+17884_1354+17886delinsTGA	NP_001353376.1:n.1354+17884_1354+17886delinsTGA
NM_001366448.1:c.1465+17884_1465+17886delinsTGA	NP_001353377.1:n.1465+17884_1465+17886delinsTGA
NM_001366449.1:c.406+17884_406+17886delinsTGA	NP_001353378.1:n.406+17884_406+17886delinsTGA
NR_158982.1:n.1636+17884_1636+17886delinsTGA
XM_005245681.2:c.1354+17884_1354+17886delinsTGA	XP_005245738.1:n.1354+17884_1354+17886delinsTGA
XM_011510223.2:c.1465+17884_1465+17886delinsTGA	XP_011508525.1:n.1465+17884_1465+17886delinsTGA
NM_014857.5:c.1465+17884_1465+17886delinsTGA	NP_055672.3:n.1465+17884_1465+17886delinsTGA