Canonical Allele Identifier: CA346974685
Gene: USP34 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.61378419T>A , CM000664.2:g.61378419T>A GRCh38
NC_000002.11:g.61605554T>A , CM000664.1:g.61605554T>A GRCh37
NC_000002.10:g.61459058T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000398571.7:c.1020A>T MANE Select ENSP00000381577.2:p.Gln340His
ENST00000398571.6:c.1020A>T ENSP00000381577.2:p.Gln340His
ENST00000453133.1:c.546A>T
NM_014709.3:c.1020A>T NP_055524.3:p.Gln340His
NM_014709.4:c.1020A>T MANE Select NP_055524.3:p.Gln340His