Canonical Allele Identifier: CA2473716778

Gene: TOE1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.45341462C= , CM000663.2:g.45341462C=	GRCh38
NC_000001.10:g.45807134C= , CM000663.1:g.45807134C=	GRCh37
NC_000001.9:g.45579721C=	NCBI36
NG_008189.1:g.4009G= , LRG_220:g.4009G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000372090.6:c.237-11C= MANE Select	ENSP00000361162.5:n.237-11C=
ENST00000671898.1:c.541-6951G=	ENSP00000499896.1:n.541-6951G=
ENST00000372090.5:c.237-11C=	ENSP00000361162.5:n.237-11C=
ENST00000460057.1:n.48+119C=
ENST00000471337.5:n.315-11C=
ENST00000477731.5:n.456-11C=
ENST00000495703.5:n.507-11C=
NM_025077.3:c.237-11C=	NP_079353.3:n.237-11C=
XM_005270412.2:c.255-11C=	XP_005270469.1:n.255-11C=
XM_005270413.3:c.99-11C=	XP_005270470.1:n.99-11C=
XM_011540569.1:c.-49+119C=	XP_011538871.1:n.-49+119C=
XR_246230.2:n.514-11C=
XR_426587.2:n.334-11C=
XR_946532.1:n.334-11C=
XM_005270412.4:c.255-11C=	XP_005270469.1:n.255-11C=
XM_005270413.5:c.99-11C=	XP_005270470.1:n.99-11C=
XM_011540569.3:c.-49+119C=	XP_011538871.1:n.-49+119C=
XM_024452837.1:c.186-11C=	XP_024308605.1:n.186-11C=
XR_001736951.2:n.424-11C=
XR_002959287.1:n.826-11C=
XR_246230.4:n.424-11C=
XR_426587.4:n.334-11C=
XR_946532.3:n.334-11C=
NM_025077.4:c.237-11C= MANE Select	NP_079353.3:n.237-11C=