Canonical Allele Identifier: CA346974473
Gene: USP34 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.61378380T>A , CM000664.2:g.61378380T>A GRCh38
NC_000002.11:g.61605515T>A , CM000664.1:g.61605515T>A GRCh37
NC_000002.10:g.61459019T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000398571.7:c.1059A>T MANE Select ENSP00000381577.2:p.Leu353Phe
ENST00000398571.6:c.1059A>T ENSP00000381577.2:p.Leu353Phe
ENST00000453133.1:c.585A>T
NM_014709.3:c.1059A>T NP_055524.3:p.Leu353Phe
NM_014709.4:c.1059A>T MANE Select NP_055524.3:p.Leu353Phe