Canonical Allele Identifier: CA48428491
Gene: USP34 HGNC NCBI

Linked Data

dbSNP Id: rs955880080
gnomAD v3: 2-61378172-CA-C
gnomAD v4: 2-61378172-CA-C
MyVariant Identifiers: chr2:g.61605308del (hg19) chr2:g.61378173del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.61378180del , CM000664.2:g.61378180del GRCh38
NC_000002.11:g.61605315del , CM000664.1:g.61605315del GRCh37
NC_000002.10:g.61458819del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000398571.7:c.1076+190del MANE Select ENSP00000381577.2:n.1076+190del
ENST00000398571.6:c.1076+190del ENSP00000381577.2:n.1076+190del
ENST00000453133.1:c.602+190del
NM_014709.3:c.1076+190del NP_055524.3:n.1076+190del
NM_014709.4:c.1076+190del MANE Select NP_055524.3:n.1076+190del
Search 100 bp 5'
Search 100 bp 3'