Canonical Allele Identifier: CA346974578

Gene: USP34

Linked Data

• MyVariant Identifiers: chr2:g.61605528T>G (hg19) ; chr2:g.61378393T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.61378393T>G , CM000664.2:g.61378393T>G	GRCh38
NC_000002.11:g.61605528T>G , CM000664.1:g.61605528T>G	GRCh37
NC_000002.10:g.61459032T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398571.7:c.1046A>C MANE Select	ENSP00000381577.2:p.Asn349Thr
ENST00000398571.6:c.1046A>C	ENSP00000381577.2:p.Asn349Thr
ENST00000453133.1:c.572A>C
NM_014709.3:c.1046A>C	NP_055524.3:p.Asn349Thr
NM_014709.4:c.1046A>C MANE Select	NP_055524.3:p.Asn349Thr