Canonical Allele Identifier: CA346974633
Gene: USP34 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.61378407G>T , CM000664.2:g.61378407G>T GRCh38
NC_000002.11:g.61605542G>T , CM000664.1:g.61605542G>T GRCh37
NC_000002.10:g.61459046G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000398571.7:c.1032C>A MANE Select ENSP00000381577.2:p.Phe344Leu
ENST00000398571.6:c.1032C>A ENSP00000381577.2:p.Phe344Leu
ENST00000453133.1:c.558C>A
NM_014709.3:c.1032C>A NP_055524.3:p.Phe344Leu
NM_014709.4:c.1032C>A MANE Select NP_055524.3:p.Phe344Leu