Canonical Allele Identifier: CA2581774457
Gene: USP34 HGNC NCBI

Linked Data

gnomAD v4: 2-61378479-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.61378479T>G , CM000664.2:g.61378479T>G GRCh38
NC_000002.11:g.61605614T>G , CM000664.1:g.61605614T>G GRCh37
NC_000002.10:g.61459118T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000398571.7:c.1015-55A>C MANE Select ENSP00000381577.2:n.1015-55A>C
ENST00000398571.6:c.1015-55A>C ENSP00000381577.2:n.1015-55A>C
ENST00000453133.1:c.541-55A>C
NM_014709.3:c.1015-55A>C NP_055524.3:n.1015-55A>C
NM_014709.4:c.1015-55A>C MANE Select NP_055524.3:n.1015-55A>C