Canonical Allele Identifier: CA475998929

Gene: GAB2 USP35

Linked Data

• MyVariant Identifiers: chr11:g.77936169T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.78225123T>C , CM000673.2:g.78225123T>C	GRCh38
NC_000011.9:g.77936169T>C , CM000673.1:g.77936169T>C	GRCh37
NC_000011.8:g.77613817T>C	NCBI36
NG_016171.1:g.197700A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361507.5:c.1287A>G (GAB2) MANE Select	ENSP00000354952.4:p.Gly429=
ENST00000340149.6:c.1173A>G (GAB2)	ENSP00000343959.2:p.Gly391=
ENST00000361507.4:c.1287A>G (GAB2)	ENSP00000354952.4:p.Gly429=
NM_012296.3:c.1173A>G (GAB2)	NP_036428.1:p.Gly391=
NM_080491.2:c.1287A>G (GAB2)	NP_536739.1:p.Gly429=
XM_006718753.1:c.1173A>G (GAB2)	XP_006718816.1:p.Gly391=
XM_011545408.1:c.627A>G (GAB2)	XP_011543710.1:p.Gly209=
XR_950117.1:n.1212A>G (GAB2)
XM_006718753.2:c.1173A>G (GAB2)	XP_006718816.1:p.Gly391=
XM_011545408.3:c.627A>G (GAB2)	XP_011543710.1:p.Gly209=
XM_024448782.1:c.1233A>G (GAB2)	XP_024304550.1:p.Gly411=
XR_001747928.1:n.3880T>C (USP35)
XR_001747930.1:n.4423T>C (USP35)
XR_001747931.1:n.3763T>C (USP35)
NM_080491.3:c.1287A>G (GAB2) MANE Select	NP_536739.1:p.Gly429=
NM_012296.4:c.1173A>G (GAB2)	NP_036428.1:p.Gly391=