Canonical Allele Identifier: CA1677656
Gene: USP34 HGNC NCBI

Linked Data

dbSNP Id: rs775380254
gnomAD v2: 2-61605517-A-G
gnomAD v4: 2-61378382-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.61378382A>G , CM000664.2:g.61378382A>G GRCh38
NC_000002.11:g.61605517A>G , CM000664.1:g.61605517A>G GRCh37
NC_000002.10:g.61459021A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000398571.7:c.1057T>C MANE Select ENSP00000381577.2:p.Leu353=
ENST00000398571.6:c.1057T>C ENSP00000381577.2:p.Leu353=
ENST00000453133.1:c.583T>C
NM_014709.3:c.1057T>C NP_055524.3:p.Leu353=
NM_014709.4:c.1057T>C MANE Select NP_055524.3:p.Leu353=