Canonical Allele Identifier: CA1586352501
Gene: UBE2D2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.139569674A= , CM000667.2:g.139569674A= GRCh38
NC_000005.9:g.138949259A= , CM000667.1:g.138949259A= GRCh37
NC_000005.8:g.138929443A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000698321.1:c.-162+7267A= ENSP00000513666.1:n.-162+7267A=
ENST00000398733.8:c.24+7859A= MANE Select ENSP00000381717.3:n.24+7859A=
ENST00000398733.7:c.24+7859A= ENSP00000381717.3:n.24+7859A=
ENST00000398734.8:c.24+7859A= ENSP00000381718.4:n.24+7859A=
ENST00000505007.5:c.-64+7267A= ENSP00000426523.1:n.-64+7267A=
ENST00000505548.5:c.-64+7267A= ENSP00000424941.1:n.-64+7267A=
ENST00000510470.1:n.92+7859A=
ENST00000511725.5:c.-63-30698A= ENSP00000429613.1:n.-63-30698A=
NM_003339.2:c.24+7859A= NP_003330.1:n.24+7859A=
NM_181838.1:c.-64+7267A= NP_862821.1:n.-64+7267A=
XM_017009820.1:c.-96+7043A= XP_016865309.1:n.-96+7043A=
NM_003339.3:c.24+7859A= MANE Select NP_003330.1:n.24+7859A=
NM_181838.2:c.-64+7267A= NP_862821.1:n.-64+7267A=