Canonical Allele Identifier: CA2563140717
Gene: USP34 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.61378150del , CM000664.2:g.61378150del GRCh38
NC_000002.11:g.61605285del , CM000664.1:g.61605285del GRCh37
NC_000002.10:g.61458789del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000398571.7:c.1076+215del MANE Select ENSP00000381577.2:n.1076+215del
ENST00000398571.6:c.1076+215del ENSP00000381577.2:n.1076+215del
ENST00000453133.1:c.602+215del
NM_014709.3:c.1076+215del NP_055524.3:n.1076+215del
NM_014709.4:c.1076+215del MANE Select NP_055524.3:n.1076+215del