Canonical Allele Identifier: CA1984593318

Gene: GAB2 USP35

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.78225132C= , CM000673.2:g.78225132C=	GRCh38
NC_000011.9:g.77936178C= , CM000673.1:g.77936178C=	GRCh37
NC_000011.8:g.77613826C=	NCBI36
NG_016171.1:g.197691G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361507.5:c.1278G= (GAB2) MANE Select	ENSP00000354952.4:p.Met426=
ENST00000340149.6:c.1164G= (GAB2)	ENSP00000343959.2:p.Met388=
ENST00000361507.4:c.1278G= (GAB2)	ENSP00000354952.4:p.Met426=
NM_012296.3:c.1164G= (GAB2)	NP_036428.1:p.Met388=
NM_080491.2:c.1278G= (GAB2)	NP_536739.1:p.Met426=
XM_006718753.1:c.1164G= (GAB2)	XP_006718816.1:p.Met388=
XM_011545408.1:c.618G= (GAB2)	XP_011543710.1:p.Met206=
XR_950117.1:n.1203G= (GAB2)
XM_006718753.2:c.1164G= (GAB2)	XP_006718816.1:p.Met388=
XM_011545408.3:c.618G= (GAB2)	XP_011543710.1:p.Met206=
XM_024448782.1:c.1224G= (GAB2)	XP_024304550.1:p.Met408=
XR_001747928.1:n.3889C= (USP35)
XR_001747930.1:n.4432C= (USP35)
XR_001747931.1:n.3772C= (USP35)
NM_080491.3:c.1278G= (GAB2) MANE Select	NP_536739.1:p.Met426=
NM_012296.4:c.1164G= (GAB2)	NP_036428.1:p.Met388=