Canonical Allele Identifier: CA2579039271

Gene: UBE2H

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.129839110G>T , CM000669.2:g.129839110G>T	GRCh38
NC_000007.13:g.129478950G>T , CM000669.1:g.129478950G>T	GRCh37
NC_000007.12:g.129266186G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355621.8:c.427+97C>A MANE Select	ENSP00000347836.3:n.427+97C>A
ENST00000649897.1:c.217+97C>A	ENSP00000497987.1:n.217+97C>A
ENST00000355621.7:c.427+97C>A	ENSP00000347836.3:n.427+97C>A
ENST00000473814.6:c.334+97C>A	ENSP00000419097.2:n.334+97C>A
ENST00000483368.1:n.535+97C>A
ENST00000496698.5:c.328+97C>A	ENSP00000417681.1:n.328+97C>A
NM_001202498.1:c.217+97C>A	NP_001189427.1:n.217+97C>A
NM_003344.3:c.427+97C>A	NP_003335.1:n.427+97C>A
NM_182697.2:c.334+97C>A	NP_874356.1:n.334+97C>A
XM_011516547.1:c.616+97C>A	XP_011514849.1:n.616+97C>A
NM_001202498.2:c.217+97C>A	NP_001189427.1:n.217+97C>A
NM_003344.4:c.427+97C>A MANE Select	NP_003335.1:n.427+97C>A
NM_182697.3:c.334+97C>A	NP_874356.1:n.334+97C>A