Canonical Allele Identifier: CA48428836
Gene: USP34 HGNC NCBI

Linked Data

dbSNP Id: rs533959590
gnomAD v3: 2-61378505-CTGAT-C
gnomAD v4: 2-61378505-CTGAT-C
MyVariant Identifiers: chr2:g.61605641_61605644del (hg19) chr2:g.61378506_61378509del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.61378509_61378512del , CM000664.2:g.61378509_61378512del GRCh38
NC_000002.11:g.61605644_61605647del , CM000664.1:g.61605644_61605647del GRCh37
NC_000002.10:g.61459148_61459151del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000398571.7:c.1015-85_1015-82del MANE Select ENSP00000381577.2:n.1015-85_1015-82del
ENST00000398571.6:c.1015-85_1015-82del ENSP00000381577.2:n.1015-85_1015-82del
ENST00000453133.1:c.541-85_541-82del
NM_014709.3:c.1015-85_1015-82del NP_055524.3:n.1015-85_1015-82del
NM_014709.4:c.1015-85_1015-82del MANE Select NP_055524.3:n.1015-85_1015-82del
Search 100 bp 5'
Search 100 bp 3'