Canonical Allele Identifier: CA382140823

Gene: GAB2 USP35

Linked Data

• MyVariant Identifiers: chr11:g.77936171C>G (hg19) ; chr11:g.78225125C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.78225125C>G , CM000673.2:g.78225125C>G	GRCh38
NC_000011.9:g.77936171C>G , CM000673.1:g.77936171C>G	GRCh37
NC_000011.8:g.77613819C>G	NCBI36
NG_016171.1:g.197698G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000361507.5:c.1285G>C (GAB2) MANE Select	ENSP00000354952.4:p.Gly429Arg
ENST00000340149.6:c.1171G>C (GAB2)	ENSP00000343959.2:p.Gly391Arg
ENST00000361507.4:c.1285G>C (GAB2)	ENSP00000354952.4:p.Gly429Arg
NM_012296.3:c.1171G>C (GAB2)	NP_036428.1:p.Gly391Arg
NM_080491.2:c.1285G>C (GAB2)	NP_536739.1:p.Gly429Arg
XM_006718753.1:c.1171G>C (GAB2)	XP_006718816.1:p.Gly391Arg
XM_011545408.1:c.625G>C (GAB2)	XP_011543710.1:p.Gly209Arg
XR_950117.1:n.1210G>C (GAB2)
XM_006718753.2:c.1171G>C (GAB2)	XP_006718816.1:p.Gly391Arg
XM_011545408.3:c.625G>C (GAB2)	XP_011543710.1:p.Gly209Arg
XM_024448782.1:c.1231G>C (GAB2)	XP_024304550.1:p.Gly411Arg
XR_001747928.1:n.3882C>G (USP35)
XR_001747930.1:n.4425C>G (USP35)
XR_001747931.1:n.3765C>G (USP35)
NM_080491.3:c.1285G>C (GAB2) MANE Select	NP_536739.1:p.Gly429Arg
NM_012296.4:c.1171G>C (GAB2)	NP_036428.1:p.Gly391Arg