Canonical Allele Identifier: CA2659222735
Gene: USP34 HGNC NCBI

Linked Data

gnomAD v4: 2-61378486-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.61378486C>A , CM000664.2:g.61378486C>A GRCh38
NC_000002.11:g.61605621C>A , CM000664.1:g.61605621C>A GRCh37
NC_000002.10:g.61459125C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000398571.7:c.1015-62G>T MANE Select ENSP00000381577.2:n.1015-62G>T
ENST00000398571.6:c.1015-62G>T ENSP00000381577.2:n.1015-62G>T
ENST00000453133.1:c.541-62G>T
NM_014709.3:c.1015-62G>T NP_055524.3:n.1015-62G>T
NM_014709.4:c.1015-62G>T MANE Select NP_055524.3:n.1015-62G>T