Canonical Allele Identifier: CA2659222740
Gene: USP34 HGNC NCBI

Linked Data

gnomAD v4: 2-61378489-A-ATAC
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.61378492_61378494dup , CM000664.2:g.61378492_61378494dup GRCh38
NC_000002.11:g.61605627_61605629dup , CM000664.1:g.61605627_61605629dup GRCh37
NC_000002.10:g.61459131_61459133dup NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000398571.7:c.1015-68_1015-66dup MANE Select ENSP00000381577.2:n.1015-68_1015-66dup
ENST00000398571.6:c.1015-68_1015-66dup ENSP00000381577.2:n.1015-68_1015-66dup
ENST00000453133.1:c.541-68_541-66dup
NM_014709.3:c.1015-68_1015-66dup NP_055524.3:n.1015-68_1015-66dup
NM_014709.4:c.1015-68_1015-66dup MANE Select NP_055524.3:n.1015-68_1015-66dup
Search 100 bp 5'
Search 100 bp 3'