Canonical Allele Identifier: CA346974688
Gene: USP34 HGNC NCBI

Linked Data

gnomAD v4: 2-61378420-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.61378420T>C , CM000664.2:g.61378420T>C GRCh38
NC_000002.11:g.61605555T>C , CM000664.1:g.61605555T>C GRCh37
NC_000002.10:g.61459059T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000398571.7:c.1019A>G MANE Select ENSP00000381577.2:p.Gln340Arg
ENST00000398571.6:c.1019A>G ENSP00000381577.2:p.Gln340Arg
ENST00000453133.1:c.545A>G
NM_014709.3:c.1019A>G NP_055524.3:p.Gln340Arg
NM_014709.4:c.1019A>G MANE Select NP_055524.3:p.Gln340Arg