Canonical Allele Identifier: CA2659222724
Gene: USP34 HGNC NCBI

Linked Data

gnomAD v4: 2-61378478-TTTGTC-T
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.61378479_61378483del , CM000664.2:g.61378479_61378483del GRCh38
NC_000002.11:g.61605614_61605618del , CM000664.1:g.61605614_61605618del GRCh37
NC_000002.10:g.61459118_61459122del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000398571.7:c.1015-59_1015-55del MANE Select ENSP00000381577.2:n.1015-59_1015-55del
ENST00000398571.6:c.1015-59_1015-55del ENSP00000381577.2:n.1015-59_1015-55del
ENST00000453133.1:c.541-59_541-55del
NM_014709.3:c.1015-59_1015-55del NP_055524.3:n.1015-59_1015-55del
NM_014709.4:c.1015-59_1015-55del MANE Select NP_055524.3:n.1015-59_1015-55del
Search 100 bp 5'
Search 100 bp 3'