Canonical Allele Identifier: CA346974652
Gene: USP34 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.61378412T>G , CM000664.2:g.61378412T>G GRCh38
NC_000002.11:g.61605547T>G , CM000664.1:g.61605547T>G GRCh37
NC_000002.10:g.61459051T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000398571.7:c.1027A>C MANE Select ENSP00000381577.2:p.Thr343Pro
ENST00000398571.6:c.1027A>C ENSP00000381577.2:p.Thr343Pro
ENST00000453133.1:c.553A>C
NM_014709.3:c.1027A>C NP_055524.3:p.Thr343Pro
NM_014709.4:c.1027A>C MANE Select NP_055524.3:p.Thr343Pro