Canonical Allele Identifier: CA1255352151

Gene: USP34

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.61378140T= , CM000664.2:g.61378140T=	GRCh38
NC_000002.11:g.61605275T= , CM000664.1:g.61605275T=	GRCh37
NC_000002.10:g.61458779T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398571.7:c.1076+223A= MANE Select	ENSP00000381577.2:n.1076+223A=
ENST00000398571.6:c.1076+223A=	ENSP00000381577.2:n.1076+223A=
ENST00000453133.1:c.602+223A=
NM_014709.3:c.1076+223A=	NP_055524.3:n.1076+223A=
NM_014709.4:c.1076+223A= MANE Select	NP_055524.3:n.1076+223A=