Canonical Allele Identifier: CA1208109226

Gene: RABGAP1L

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.174322906G= , CM000663.2:g.174322906G=	GRCh38
NC_000001.10:g.174292044G= , CM000663.1:g.174292044G=	GRCh37
NC_000001.9:g.172558667G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681986.1:c.1465+17779G= MANE Select	ENSP00000507884.1:n.1465+17779G=
ENST00000251507.8:c.1465+17779G=	ENSP00000251507.4:n.1465+17779G=
ENST00000357444.10:c.1354+17779G=	ENSP00000350027.6:n.1354+17779G=
ENST00000367690.5:c.406+17779G=	ENSP00000489605.1:n.406+17779G=
ENST00000457696.1:c.1501+17779G=	ENSP00000403136.1:n.1501+17779G=
NM_014857.4:c.1465+17779G=	NP_055672.3:n.1465+17779G=
XM_005245680.1:c.1465+17779G=	XP_005245737.1:n.1465+17779G=
XM_005245681.1:c.1354+17779G=	XP_005245738.1:n.1354+17779G=
XM_006711693.1:c.1465+17779G=	XP_006711756.1:n.1465+17779G=
XM_011510223.1:c.1465+17779G=	XP_011508525.1:n.1465+17779G=
XR_922003.1:n.1672+17779G=
XR_922004.1:n.1672+17779G=
NM_001366445.1:c.1354+17779G=	NP_001353374.1:n.1354+17779G=
NM_001366446.1:c.1465+17779G= MANE Select	NP_001353375.1:n.1465+17779G=
NM_001366447.1:c.1354+17779G=	NP_001353376.1:n.1354+17779G=
NM_001366448.1:c.1465+17779G=	NP_001353377.1:n.1465+17779G=
NM_001366449.1:c.406+17779G=	NP_001353378.1:n.406+17779G=
NR_158982.1:n.1636+17779G=
XM_005245681.2:c.1354+17779G=	XP_005245738.1:n.1354+17779G=
XM_011510223.2:c.1465+17779G=	XP_011508525.1:n.1465+17779G=
NM_014857.5:c.1465+17779G=	NP_055672.3:n.1465+17779G=