Canonical Allele Identifier: CA1255352393
Gene: USP34 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.61378601_61378606delinsGTTATA , CM000664.2:g.61378601_61378606delinsGTTATA GRCh38
NC_000002.11:g.61605736_61605741delinsGTTATA , CM000664.1:g.61605736_61605741delinsGTTATA GRCh37
NC_000002.10:g.61459240_61459245delinsGTTATA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000398571.7:c.1015-182_1015-177delinsTATAAC MANE Select ENSP00000381577.2:n.1015-182_1015-177delinsTATAAC
ENST00000398571.6:c.1015-182_1015-177delinsTATAAC ENSP00000381577.2:n.1015-182_1015-177delinsTATAAC
ENST00000453133.1:c.541-182_541-177delinsTATAAC
NM_014709.3:c.1015-182_1015-177delinsTATAAC NP_055524.3:n.1015-182_1015-177delinsTATAAC
NM_014709.4:c.1015-182_1015-177delinsTATAAC MANE Select NP_055524.3:n.1015-182_1015-177delinsTATAAC