Canonical Allele Identifier: CA2454589985

Gene: UBE2A

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.119583178C= , CM000685.2:g.119583178C=	GRCh38
NC_000023.10:g.118717141C= , CM000685.1:g.118717141C=	GRCh37
NC_000023.9:g.118601169C=	NCBI36
NG_009267.1:g.13643C=

Transcript Alleles

HGVS	Amino-acid Change
NM_003336.4:c.382C= MANE Select	NP_003327.2:p.Gln128=
ENST00000371558.7:c.382C= MANE Select	ENSP00000360613.2:p.Gln128=
NM_001282161.1:c.283C=	NP_001269090.1:p.Gln95=
NM_001282161.2:c.283C=	NP_001269090.1:p.Gln95=
NM_003336.3:c.382C=	NP_003327.2:p.Gln128=
NM_181762.2:c.292C=	NP_861427.1:p.Gln98=
NM_181762.3:c.292C=	NP_861427.1:p.Gln98=
ENST00000346330.6:c.373C=	ENSP00000335027.4:p.Gln125=
ENST00000371558.6:c.382C=	ENSP00000360613.2:p.Gln128=
ENST00000371569.6:n.1403C=
ENST00000625938.2:c.292C=	ENSP00000486599.1:p.Gln98=
ENST00000628549.1:c.283C=	ENSP00000487203.1:p.Gln95=
ENST00000628734.1:n.361C=
ENST00000630695.2:c.157C=	ENSP00000486550.1:p.Gln53=
ENST00000631185.2:c.330+502C=	ENSP00000486153.1:n.330+502C=
ENST00000696533.1:c.598C=	ENSP00000512694.1:p.Gln200=
ENST00000696534.1:c.382C=	ENSP00000512695.1:p.Gln128=
ENST00000696539.1:c.598C=	ENSP00000512700.1:p.Gln200=