Canonical Allele Identifier: CA1255352388

Gene: USP34

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.61378593C= , CM000664.2:g.61378593C=	GRCh38
NC_000002.11:g.61605728C= , CM000664.1:g.61605728C=	GRCh37
NC_000002.10:g.61459232C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398571.7:c.1015-169G= MANE Select	ENSP00000381577.2:n.1015-169G=
ENST00000398571.6:c.1015-169G=	ENSP00000381577.2:n.1015-169G=
ENST00000453133.1:c.541-169G=
NM_014709.3:c.1015-169G=	NP_055524.3:n.1015-169G=
NM_014709.4:c.1015-169G= MANE Select	NP_055524.3:n.1015-169G=