Canonical Allele Identifier: CA369449042

Gene: UBE2H

Linked Data

• MyVariant Identifiers: chr7:g.129479055T>C (hg19) ; chr7:g.129839215T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.129839215T>C , CM000669.2:g.129839215T>C	GRCh38
NC_000007.13:g.129479055T>C , CM000669.1:g.129479055T>C	GRCh37
NC_000007.12:g.129266291T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000355621.8:c.419A>G MANE Select	ENSP00000347836.3:p.Lys140Arg
ENST00000649897.1:c.209A>G	ENSP00000497987.1:p.Lys70Arg
ENST00000355621.7:c.419A>G	ENSP00000347836.3:p.Lys140Arg
ENST00000472396.5:c.359A>G	ENSP00000419689.1:p.Lys120Arg
ENST00000473814.6:c.326A>G	ENSP00000419097.2:p.Lys109Arg
ENST00000483368.1:n.527A>G
ENST00000496698.5:c.320A>G	ENSP00000417681.1:p.Lys107Arg
NM_001202498.1:c.209A>G	NP_001189427.1:p.Lys70Arg
NM_003344.3:c.419A>G	NP_003335.1:p.Lys140Arg
NM_182697.2:c.326A>G	NP_874356.1:p.Lys109Arg
XM_011516547.1:c.608A>G	XP_011514849.1:p.Lys203Arg
NM_001202498.2:c.209A>G	NP_001189427.1:p.Lys70Arg
NM_003344.4:c.419A>G MANE Select	NP_003335.1:p.Lys140Arg
NM_182697.3:c.326A>G	NP_874356.1:p.Lys109Arg