Canonical Allele Identifier: CA1984621032

Gene: GAB2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.78281948A= , CM000673.2:g.78281948A=	GRCh38
NC_000011.9:g.77992994A= , CM000673.1:g.77992994A=	GRCh37
NC_000011.8:g.77670642A=	NCBI36
NG_016171.1:g.140875T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361507.5:c.76-1047T= MANE Select	ENSP00000354952.4:n.76-1047T=
ENST00000340149.6:c.-39-1047T=	ENSP00000343959.2:n.-39-1047T=
ENST00000361507.4:c.76-1047T=	ENSP00000354952.4:n.76-1047T=
ENST00000526030.1:n.255-1047T=
ENST00000528886.5:c.-39-1047T=	ENSP00000433762.1:n.-39-1047T=
ENST00000530915.1:c.-39-1047T=	ENSP00000431868.1:n.-39-1047T=
ENST00000534823.1:n.127-1047T=
NM_012296.3:c.-39-1047T=	NP_036428.1:n.-39-1047T=
NM_080491.2:c.76-1047T=	NP_536739.1:n.76-1047T=
XM_006718753.1:c.-39-1047T=	XP_006718816.1:n.-39-1047T=
XM_011545408.1:c.-341-1047T=	XP_011543710.1:n.-341-1047T=
XM_006718753.2:c.-39-1047T=	XP_006718816.1:n.-39-1047T=
XM_011545408.3:c.-341-1047T=	XP_011543710.1:n.-341-1047T=
XM_024448782.1:c.22-1047T=	XP_024304550.1:n.22-1047T=
NM_080491.3:c.76-1047T= MANE Select	NP_536739.1:n.76-1047T=
NM_012296.4:c.-39-1047T=	NP_036428.1:n.-39-1047T=