Canonical Allele Identifier: CA2838625368
Gene: USP34 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.61378479_61378480del , CM000664.2:g.61378479_61378480del GRCh38
NC_000002.11:g.61605614_61605615del , CM000664.1:g.61605614_61605615del GRCh37
NC_000002.10:g.61459118_61459119del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000398571.7:c.1015-55_1015-54del MANE Select ENSP00000381577.2:n.1015-55_1015-54del
ENST00000398571.6:c.1015-55_1015-54del ENSP00000381577.2:n.1015-55_1015-54del
ENST00000453133.1:c.541-55_541-54del
NM_014709.3:c.1015-55_1015-54del NP_055524.3:n.1015-55_1015-54del
NM_014709.4:c.1015-55_1015-54del MANE Select NP_055524.3:n.1015-55_1015-54del