Canonical Allele Identifier: CA1743017335
Gene: UBE2H HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.129839210T= , CM000669.2:g.129839210T= GRCh38
NC_000007.13:g.129479050T= , CM000669.1:g.129479050T= GRCh37
NC_000007.12:g.129266286T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000355621.8:c.424A= MANE Select ENSP00000347836.3:p.Lys142=
ENST00000649897.1:c.214A= ENSP00000497987.1:p.Lys72=
ENST00000355621.7:c.424A= ENSP00000347836.3:p.Lys142=
ENST00000472396.5:c.364A= ENSP00000419689.1:p.Lys122=
ENST00000473814.6:c.331A= ENSP00000419097.2:p.Lys111=
ENST00000483368.1:n.532A=
ENST00000496698.5:c.325A= ENSP00000417681.1:p.Lys109=
NM_001202498.1:c.214A= NP_001189427.1:p.Lys72=
NM_003344.3:c.424A= NP_003335.1:p.Lys142=
NM_182697.2:c.331A= NP_874356.1:p.Lys111=
XM_011516547.1:c.613A= XP_011514849.1:p.Lys205=
NM_001202498.2:c.214A= NP_001189427.1:p.Lys72=
NM_003344.4:c.424A= MANE Select NP_003335.1:p.Lys142=
NM_182697.3:c.331A= NP_874356.1:p.Lys111=