Canonical Allele Identifier: CA2062452836

Gene: UBE3B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109521540G= , CM000674.2:g.109521540G=	GRCh38
NC_000012.11:g.109959345G= , CM000674.1:g.109959345G=	GRCh37
NC_000012.10:g.108443728G=	NCBI36
NG_033898.1:g.48918G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342494.8:c.2353G= MANE Select	ENSP00000340596.3:p.Ala785=
ENST00000342494.7:c.2353G=	ENSP00000340596.3:p.Ala785=
ENST00000434735.6:c.2353G=	ENSP00000391529.2:p.Ala785=
ENST00000449510.6:c.*323G=	ENSP00000395802.2:n.*323G=
ENST00000538070.1:n.1869G=
ENST00000539584.5:n.1877G=
ENST00000539599.5:c.2353G=	ENSP00000443131.1:p.Ala785=
NM_130466.3:c.2353G=	NP_569733.2:p.Ala785=
NM_183415.2:c.2353G=	NP_904324.1:p.Ala785=
XM_005253987.1:c.2353G=	XP_005254044.1:p.Ala785=
XM_006719681.2:c.2353G=	XP_006719744.1:p.Ala785=
XM_006719682.1:c.2353G=	XP_006719745.1:p.Ala785=
XM_011538959.1:c.2353G=	XP_011537261.1:p.Ala785=
XM_011538960.1:c.2353G=	XP_011537262.1:p.Ala785=
XM_011538961.1:c.2353G=	XP_011537263.1:p.Ala785=
XM_011538962.1:c.2353G=	XP_011537264.1:p.Ala785=
XR_429118.2:n.3180G=
XM_005253987.2:c.2353G=	XP_005254044.1:p.Ala785=
XM_006719681.3:c.2353G=	XP_006719744.1:p.Ala785=
XM_006719682.2:c.2353G=	XP_006719745.1:p.Ala785=
XM_011538959.2:c.2353G=	XP_011537261.1:p.Ala785=
XM_017020195.1:c.1774G=	XP_016875684.1:p.Ala592=
XM_024449269.1:c.1774G=	XP_024305037.1:p.Ala592=
XR_429118.3:n.3180G=
XR_429119.4:n.3369G=
NM_130466.4:c.2353G= MANE Select	NP_569733.2:p.Ala785=
NM_183415.3:c.2353G=	NP_904324.1:p.Ala785=