Canonical Allele Identifier: CA1255352364
Gene: USP34 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.61378528_61378532delinsATAAC , CM000664.2:g.61378528_61378532delinsATAAC GRCh38
NC_000002.11:g.61605663_61605667delinsATAAC , CM000664.1:g.61605663_61605667delinsATAAC GRCh37
NC_000002.10:g.61459167_61459171delinsATAAC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000398571.7:c.1015-108_1015-104delinsGTTAT MANE Select ENSP00000381577.2:n.1015-108_1015-104delinsGTTAT
ENST00000398571.6:c.1015-108_1015-104delinsGTTAT ENSP00000381577.2:n.1015-108_1015-104delinsGTTAT
ENST00000453133.1:c.541-108_541-104delinsGTTAT
NM_014709.3:c.1015-108_1015-104delinsGTTAT NP_055524.3:n.1015-108_1015-104delinsGTTAT
NM_014709.4:c.1015-108_1015-104delinsGTTAT MANE Select NP_055524.3:n.1015-108_1015-104delinsGTTAT