Canonical Allele Identifier: CA382140838

Gene: GAB2 USP35

Linked Data

• dbSNP Id: rs969758248
• MyVariant Identifiers: chr11:g.77936174C>A (hg19) ; chr11:g.78225128C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.78225128C>A , CM000673.2:g.78225128C>A	GRCh38
NC_000011.9:g.77936174C>A , CM000673.1:g.77936174C>A	GRCh37
NC_000011.8:g.77613822C>A	NCBI36
NG_016171.1:g.197695G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000361507.5:c.1282G>T (GAB2) MANE Select	ENSP00000354952.4:p.Asp428Tyr
ENST00000340149.6:c.1168G>T (GAB2)	ENSP00000343959.2:p.Asp390Tyr
ENST00000361507.4:c.1282G>T (GAB2)	ENSP00000354952.4:p.Asp428Tyr
NM_012296.3:c.1168G>T (GAB2)	NP_036428.1:p.Asp390Tyr
NM_080491.2:c.1282G>T (GAB2)	NP_536739.1:p.Asp428Tyr
XM_006718753.1:c.1168G>T (GAB2)	XP_006718816.1:p.Asp390Tyr
XM_011545408.1:c.622G>T (GAB2)	XP_011543710.1:p.Asp208Tyr
XR_950117.1:n.1207G>T (GAB2)
XM_006718753.2:c.1168G>T (GAB2)	XP_006718816.1:p.Asp390Tyr
XM_011545408.3:c.622G>T (GAB2)	XP_011543710.1:p.Asp208Tyr
XM_024448782.1:c.1228G>T (GAB2)	XP_024304550.1:p.Asp410Tyr
XR_001747928.1:n.3885C>A (USP35)
XR_001747930.1:n.4428C>A (USP35)
XR_001747931.1:n.3768C>A (USP35)
NM_080491.3:c.1282G>T (GAB2) MANE Select	NP_536739.1:p.Asp428Tyr
NM_012296.4:c.1168G>T (GAB2)	NP_036428.1:p.Asp390Tyr