Canonical Allele Identifier: CA346974500
Gene: USP34 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.61378385A>C , CM000664.2:g.61378385A>C GRCh38
NC_000002.11:g.61605520A>C , CM000664.1:g.61605520A>C GRCh37
NC_000002.10:g.61459024A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000398571.7:c.1054T>G MANE Select ENSP00000381577.2:p.Ser352Ala
ENST00000398571.6:c.1054T>G ENSP00000381577.2:p.Ser352Ala
ENST00000453133.1:c.580T>G
NM_014709.3:c.1054T>G NP_055524.3:p.Ser352Ala
NM_014709.4:c.1054T>G MANE Select NP_055524.3:p.Ser352Ala