Canonical Allele Identifier: CA1255352289
Gene: USP34 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.61378387T= , CM000664.2:g.61378387T= GRCh38
NC_000002.11:g.61605522T= , CM000664.1:g.61605522T= GRCh37
NC_000002.10:g.61459026T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000398571.7:c.1052A= MANE Select ENSP00000381577.2:p.Glu351=
ENST00000398571.6:c.1052A= ENSP00000381577.2:p.Glu351=
ENST00000453133.1:c.578A=
NM_014709.3:c.1052A= NP_055524.3:p.Glu351=
NM_014709.4:c.1052A= MANE Select NP_055524.3:p.Glu351=