Canonical Allele Identifier: CA1255352232
Gene: USP34 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.61378291A= , CM000664.2:g.61378291A= GRCh38
NC_000002.11:g.61605426A= , CM000664.1:g.61605426A= GRCh37
NC_000002.10:g.61458930A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000398571.7:c.1076+72T= MANE Select ENSP00000381577.2:n.1076+72T=
ENST00000398571.6:c.1076+72T= ENSP00000381577.2:n.1076+72T=
ENST00000453133.1:c.602+72T=
NM_014709.3:c.1076+72T= NP_055524.3:n.1076+72T=
NM_014709.4:c.1076+72T= MANE Select NP_055524.3:n.1076+72T=