Canonical Allele Identifier: CA382140848

Gene: GAB2 USP35

Linked Data

• dbSNP Id: rs1864588929
• MyVariant Identifiers: chr11:g.77936176C>G (hg19) ; chr11:g.78225130C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.78225130C>G , CM000673.2:g.78225130C>G	GRCh38
NC_000011.9:g.77936176C>G , CM000673.1:g.77936176C>G	GRCh37
NC_000011.8:g.77613824C>G	NCBI36
NG_016171.1:g.197693G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000361507.5:c.1280G>C (GAB2) MANE Select	ENSP00000354952.4:p.Ser427Thr
ENST00000340149.6:c.1166G>C (GAB2)	ENSP00000343959.2:p.Ser389Thr
ENST00000361507.4:c.1280G>C (GAB2)	ENSP00000354952.4:p.Ser427Thr
NM_012296.3:c.1166G>C (GAB2)	NP_036428.1:p.Ser389Thr
NM_080491.2:c.1280G>C (GAB2)	NP_536739.1:p.Ser427Thr
XM_006718753.1:c.1166G>C (GAB2)	XP_006718816.1:p.Ser389Thr
XM_011545408.1:c.620G>C (GAB2)	XP_011543710.1:p.Ser207Thr
XR_950117.1:n.1205G>C (GAB2)
XM_006718753.2:c.1166G>C (GAB2)	XP_006718816.1:p.Ser389Thr
XM_011545408.3:c.620G>C (GAB2)	XP_011543710.1:p.Ser207Thr
XM_024448782.1:c.1226G>C (GAB2)	XP_024304550.1:p.Ser409Thr
XR_001747928.1:n.3887C>G (USP35)
XR_001747930.1:n.4430C>G (USP35)
XR_001747931.1:n.3770C>G (USP35)
NM_080491.3:c.1280G>C (GAB2) MANE Select	NP_536739.1:p.Ser427Thr
NM_012296.4:c.1166G>C (GAB2)	NP_036428.1:p.Ser389Thr