Canonical Allele Identifier: CA1743017384
Gene: UBE2H HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.129839298T= , CM000669.2:g.129839298T= GRCh38
NC_000007.13:g.129479138T= , CM000669.1:g.129479138T= GRCh37
NC_000007.12:g.129266374T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000355621.8:c.336A= MANE Select ENSP00000347836.3:p.Leu112=
ENST00000649897.1:c.126A= ENSP00000497987.1:p.Leu42=
ENST00000355621.7:c.336A= ENSP00000347836.3:p.Leu112=
ENST00000472396.5:c.299-23A= ENSP00000419689.1:n.299-23A=
ENST00000473814.6:c.243A= ENSP00000419097.2:p.Leu81=
ENST00000480245.5:c.363A= ENSP00000417709.1:n.363A=
ENST00000483368.1:n.444A=
ENST00000496698.5:c.237A= ENSP00000417681.1:p.Leu79=
NM_001202498.1:c.126A= NP_001189427.1:p.Leu42=
NM_003344.3:c.336A= NP_003335.1:p.Leu112=
NM_182697.2:c.243A= NP_874356.1:p.Leu81=
XM_011516547.1:c.525A= XP_011514849.1:p.Leu175=
NM_001202498.2:c.126A= NP_001189427.1:p.Leu42=
NM_003344.4:c.336A= MANE Select NP_003335.1:p.Leu112=
NM_182697.3:c.243A= NP_874356.1:p.Leu81=