Canonical Allele Identifier: CA1148243224

Gene: TOE1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.45341458A= , CM000663.2:g.45341458A=	GRCh38
NC_000001.10:g.45807130A= , CM000663.1:g.45807130A=	GRCh37
NC_000001.9:g.45579717A=	NCBI36
NG_008189.1:g.4013T= , LRG_220:g.4013T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000372090.6:c.237-15A= MANE Select	ENSP00000361162.5:n.237-15A=
ENST00000671898.1:c.541-6947T=	ENSP00000499896.1:n.541-6947T=
ENST00000372090.5:c.237-15A=	ENSP00000361162.5:n.237-15A=
ENST00000460057.1:n.48+115A=
ENST00000471337.5:n.315-15A=
ENST00000477731.5:n.456-15A=
ENST00000495703.5:n.507-15A=
NM_025077.3:c.237-15A=	NP_079353.3:n.237-15A=
XM_005270412.2:c.255-15A=	XP_005270469.1:n.255-15A=
XM_005270413.3:c.99-15A=	XP_005270470.1:n.99-15A=
XM_011540569.1:c.-49+115A=	XP_011538871.1:n.-49+115A=
XR_246230.2:n.514-15A=
XR_426587.2:n.334-15A=
XR_946532.1:n.334-15A=
XM_005270412.4:c.255-15A=	XP_005270469.1:n.255-15A=
XM_005270413.5:c.99-15A=	XP_005270470.1:n.99-15A=
XM_011540569.3:c.-49+115A=	XP_011538871.1:n.-49+115A=
XM_024452837.1:c.186-15A=	XP_024308605.1:n.186-15A=
XR_001736951.2:n.424-15A=
XR_002959287.1:n.826-15A=
XR_246230.4:n.424-15A=
XR_426587.4:n.334-15A=
XR_946532.3:n.334-15A=
NM_025077.4:c.237-15A= MANE Select	NP_079353.3:n.237-15A=