Canonical Allele Identifier: CA1255352261
Gene: USP34 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.61378332T= , CM000664.2:g.61378332T= GRCh38
NC_000002.11:g.61605467T= , CM000664.1:g.61605467T= GRCh37
NC_000002.10:g.61458971T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000398571.7:c.1076+31A= MANE Select ENSP00000381577.2:n.1076+31A=
ENST00000398571.6:c.1076+31A= ENSP00000381577.2:n.1076+31A=
ENST00000453133.1:c.602+31A=
NM_014709.3:c.1076+31A= NP_055524.3:n.1076+31A=
NM_014709.4:c.1076+31A= MANE Select NP_055524.3:n.1076+31A=