Canonical Allele Identifier: CA2659222717
Gene: USP34 HGNC NCBI

Linked Data

gnomAD v4: 2-61378473-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.61378473T>G , CM000664.2:g.61378473T>G GRCh38
NC_000002.11:g.61605608T>G , CM000664.1:g.61605608T>G GRCh37
NC_000002.10:g.61459112T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000398571.7:c.1015-49A>C MANE Select ENSP00000381577.2:n.1015-49A>C
ENST00000398571.6:c.1015-49A>C ENSP00000381577.2:n.1015-49A>C
ENST00000453133.1:c.541-49A>C
NM_014709.3:c.1015-49A>C NP_055524.3:n.1015-49A>C
NM_014709.4:c.1015-49A>C MANE Select NP_055524.3:n.1015-49A>C
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