Canonical Allele Identifier: CA1143822421

Gene: TOE1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.45341543G= , CM000663.2:g.45341543G=	GRCh38
NC_000001.10:g.45807215G= , CM000663.1:g.45807215G=	GRCh37
NC_000001.9:g.45579802G=	NCBI36
NG_008189.1:g.3928C= , LRG_220:g.3928C=

Transcript Alleles

HGVS	Amino-acid Change
NM_025077.4:c.307G= MANE Select	NP_079353.3:p.Ala103=
ENST00000372090.6:c.307G= MANE Select	ENSP00000361162.5:p.Ala103=
NM_025077.3:c.307G=	NP_079353.3:p.Ala103=
ENST00000372090.5:c.307G=	ENSP00000361162.5:p.Ala103=
ENST00000460057.1:n.48+200G=
ENST00000471337.5:n.385G=
ENST00000477731.5:n.526G=
ENST00000495703.5:n.577G=
ENST00000671898.1:c.541-7032C=	ENSP00000499896.1:n.541-7032C=
XM_005270412.2:c.325G=	XP_005270469.1:p.Ala109=
XM_005270412.4:c.325G=	XP_005270469.1:p.Ala109=
XM_005270413.3:c.169G=	XP_005270470.1:p.Ala57=
XM_005270413.5:c.169G=	XP_005270470.1:p.Ala57=
XM_011540569.1:c.-49+200G=	XP_011538871.1:n.-49+200G=
XM_011540569.3:c.-49+200G=	XP_011538871.1:n.-49+200G=
XM_024452837.1:c.256G=	XP_024308605.1:p.Ala86=
XR_001736951.2:n.494G=
XR_002959287.1:n.896G=
XR_246230.2:n.584G=
XR_246230.4:n.494G=
XR_426587.2:n.404G=
XR_426587.4:n.404G=
XR_946532.1:n.404G=
XR_946532.3:n.404G=