Canonical Allele Identifier: CA1500170810

Gene: GAB1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.143438337C= , CM000666.2:g.143438337C=	GRCh38
NC_000004.11:g.144359490C= , CM000666.1:g.144359490C=	GRCh37
NC_000004.10:g.144578940C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262995.9:c.932C=	ENSP00000262995.4:p.Pro311=
ENST00000262994.9:c.932C= MANE Select	ENSP00000262994.4:p.Pro311=
ENST00000262994.8:c.932C=	ENSP00000262994.4:p.Pro311=
ENST00000262995.8:c.932C=	ENSP00000262995.4:p.Pro311=
ENST00000505913.5:c.623C=	ENSP00000424554.1:p.Pro208=
ENST00000507334.1:n.81C=
ENST00000512843.1:c.226+4621C=
NM_002039.3:c.932C=	NP_002030.2:p.Pro311=
NM_207123.2:c.932C=	NP_997006.1:p.Pro311=
XM_005262881.3:c.1013C=	XP_005262938.1:p.Pro338=
XM_005262882.3:c.1013C=	XP_005262939.1:p.Pro338=
XM_006714167.2:c.704C=	XP_006714230.1:p.Pro235=
XM_006714168.2:c.704C=	XP_006714231.1:p.Pro235=
XM_006714167.4:c.704C=	XP_006714230.1:p.Pro235=
XM_006714168.4:c.704C=	XP_006714231.1:p.Pro235=
XM_017007966.1:c.974C=	XP_016863455.1:p.Pro325=
XM_017007967.1:c.962C=	XP_016863456.1:p.Pro321=
XM_017007968.1:c.893C=	XP_016863457.1:p.Pro298=
XM_017007969.1:c.704C=	XP_016863458.1:p.Pro235=
XM_017007970.1:c.704C=	XP_016863459.1:p.Pro235=
XM_017007971.1:c.623C=	XP_016863460.1:p.Pro208=
NM_002039.4:c.932C= MANE Select	NP_002030.2:p.Pro311=
NM_207123.3:c.932C=	NP_997006.1:p.Pro311=