Canonical Allele Identifier: CA346974480
Gene: USP34 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.61378381A>G , CM000664.2:g.61378381A>G GRCh38
NC_000002.11:g.61605516A>G , CM000664.1:g.61605516A>G GRCh37
NC_000002.10:g.61459020A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000398571.7:c.1058T>C MANE Select ENSP00000381577.2:p.Leu353Ser
ENST00000398571.6:c.1058T>C ENSP00000381577.2:p.Leu353Ser
ENST00000453133.1:c.584T>C
NM_014709.3:c.1058T>C NP_055524.3:p.Leu353Ser
NM_014709.4:c.1058T>C MANE Select NP_055524.3:p.Leu353Ser