Canonical Allele Identifier: CA2659222725
Gene: USP34 HGNC NCBI

Linked Data

gnomAD v4: 2-61378479-TTGTCAGCAA-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.61378480_61378488del , CM000664.2:g.61378480_61378488del GRCh38
NC_000002.11:g.61605615_61605623del , CM000664.1:g.61605615_61605623del GRCh37
NC_000002.10:g.61459119_61459127del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000398571.7:c.1015-64_1015-56del MANE Select ENSP00000381577.2:n.1015-64_1015-56del
ENST00000398571.6:c.1015-64_1015-56del ENSP00000381577.2:n.1015-64_1015-56del
ENST00000453133.1:c.541-64_541-56del
NM_014709.3:c.1015-64_1015-56del NP_055524.3:n.1015-64_1015-56del
NM_014709.4:c.1015-64_1015-56del MANE Select NP_055524.3:n.1015-64_1015-56del
Search 100 bp 5'
Search 100 bp 3'