Canonical Allele Identifier: CA2684877435
Gene: UBE2H HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.129839145dup , CM000669.2:g.129839145dup GRCh38
NC_000007.13:g.129478985dup , CM000669.1:g.129478985dup GRCh37
NC_000007.12:g.129266221dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000355621.8:c.427+63dup MANE Select ENSP00000347836.3:n.427+63dup
ENST00000649897.1:c.217+63dup ENSP00000497987.1:n.217+63dup
ENST00000355621.7:c.427+63dup ENSP00000347836.3:n.427+63dup
ENST00000473814.6:c.334+63dup ENSP00000419097.2:n.334+63dup
ENST00000483368.1:n.535+63dup
ENST00000496698.5:c.328+63dup ENSP00000417681.1:n.328+63dup
NM_001202498.1:c.217+63dup NP_001189427.1:n.217+63dup
NM_003344.3:c.427+63dup NP_003335.1:n.427+63dup
NM_182697.2:c.334+63dup NP_874356.1:n.334+63dup
XM_011516547.1:c.616+63dup XP_011514849.1:n.616+63dup
NM_001202498.2:c.217+63dup NP_001189427.1:n.217+63dup
NM_003344.4:c.427+63dup MANE Select NP_003335.1:n.427+63dup
NM_182697.3:c.334+63dup NP_874356.1:n.334+63dup