Canonical Allele Identifier: CA382140866

Gene: GAB2 USP35

Linked Data

• dbSNP Id: rs2134464074
• MyVariant Identifiers: chr11:g.77936179A>T (hg19) ; chr11:g.78225133A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.78225133A>T , CM000673.2:g.78225133A>T	GRCh38
NC_000011.9:g.77936179A>T , CM000673.1:g.77936179A>T	GRCh37
NC_000011.8:g.77613827A>T	NCBI36
NG_016171.1:g.197690T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000361507.5:c.1277T>A (GAB2) MANE Select	ENSP00000354952.4:p.Met426Lys
ENST00000340149.6:c.1163T>A (GAB2)	ENSP00000343959.2:p.Met388Lys
ENST00000361507.4:c.1277T>A (GAB2)	ENSP00000354952.4:p.Met426Lys
NM_012296.3:c.1163T>A (GAB2)	NP_036428.1:p.Met388Lys
NM_080491.2:c.1277T>A (GAB2)	NP_536739.1:p.Met426Lys
XM_006718753.1:c.1163T>A (GAB2)	XP_006718816.1:p.Met388Lys
XM_011545408.1:c.617T>A (GAB2)	XP_011543710.1:p.Met206Lys
XR_950117.1:n.1202T>A (GAB2)
XM_006718753.2:c.1163T>A (GAB2)	XP_006718816.1:p.Met388Lys
XM_011545408.3:c.617T>A (GAB2)	XP_011543710.1:p.Met206Lys
XM_024448782.1:c.1223T>A (GAB2)	XP_024304550.1:p.Met408Lys
XR_001747928.1:n.3890A>T (USP35)
XR_001747930.1:n.4433A>T (USP35)
XR_001747931.1:n.3773A>T (USP35)
NM_080491.3:c.1277T>A (GAB2) MANE Select	NP_536739.1:p.Met426Lys
NM_012296.4:c.1163T>A (GAB2)	NP_036428.1:p.Met388Lys