Canonical Allele Identifier: CA1208221145

Gene: RABGAP1L

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.174583624G= , CM000663.2:g.174583624G=	GRCh38
NC_000001.10:g.174552762G= , CM000663.1:g.174552762G=	GRCh37
NC_000001.9:g.172819385G=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000681986.1:c.1711-53751G= MANE Select	ENSP00000507884.1:n.1711-53751G=
ENST00000251507.8:c.1711-53751G=	ENSP00000251507.4:n.1711-53751G=
ENST00000526253.1:n.326-53751G=
NM_014857.4:c.1711-53751G=	NP_055672.3:n.1711-53751G=
XM_005245680.1:c.1711-53751G=	XP_005245737.1:n.1711-53751G=
XM_005245681.1:c.1600-53751G=	XP_005245738.1:n.1600-53751G=
XM_006711693.1:c.1711-53751G=	XP_006711756.1:n.1711-53751G=
XM_011510223.1:c.1711-53751G=	XP_011508525.1:n.1711-53751G=
XR_922003.1:n.1918-53751G=
XR_922004.1:n.1918-53751G=
NM_001366446.1:c.1711-53751G= MANE Select	NP_001353375.1:n.1711-53751G=
NM_001366447.1:c.1600-53751G=	NP_001353376.1:n.1600-53751G=
NM_001366448.1:c.1711-53751G=	NP_001353377.1:n.1711-53751G=
NR_158982.1:n.1882-53751G=
XM_005245681.2:c.1600-53751G=	XP_005245738.1:n.1600-53751G=
XM_011510223.2:c.1711-53751G=	XP_011508525.1:n.1711-53751G=
NM_014857.5:c.1711-53751G=	NP_055672.3:n.1711-53751G=