Canonical Allele Identifier: CA1255352155

Gene: USP34

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.61378150G= , CM000664.2:g.61378150G=	GRCh38
NC_000002.11:g.61605285G= , CM000664.1:g.61605285G=	GRCh37
NC_000002.10:g.61458789G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398571.7:c.1076+213C= MANE Select	ENSP00000381577.2:n.1076+213C=
ENST00000398571.6:c.1076+213C=	ENSP00000381577.2:n.1076+213C=
ENST00000453133.1:c.602+213C=
NM_014709.3:c.1076+213C=	NP_055524.3:n.1076+213C=
NM_014709.4:c.1076+213C= MANE Select	NP_055524.3:n.1076+213C=