Canonical Allele Identifier: CA2473716779
Gene: TOE1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45341463C= , CM000663.2:g.45341463C= GRCh38
NC_000001.10:g.45807135C= , CM000663.1:g.45807135C= GRCh37
NC_000001.9:g.45579722C= NCBI36
NG_008189.1:g.4008G= , LRG_220:g.4008G=

Transcript Alleles

HGVS Amino-acid change
ENST00000372090.6:c.237-10C= MANE Select ENSP00000361162.5:n.237-10C=
ENST00000671898.1:c.541-6952G= ENSP00000499896.1:n.541-6952G=
ENST00000372090.5:c.237-10C= ENSP00000361162.5:n.237-10C=
ENST00000460057.1:n.48+120C=
ENST00000471337.5:n.315-10C=
ENST00000477731.5:n.456-10C=
ENST00000495703.5:n.507-10C=
NM_025077.3:c.237-10C= NP_079353.3:n.237-10C=
XM_005270412.2:c.255-10C= XP_005270469.1:n.255-10C=
XM_005270413.3:c.99-10C= XP_005270470.1:n.99-10C=
XM_011540569.1:c.-49+120C= XP_011538871.1:n.-49+120C=
XR_246230.2:n.514-10C=
XR_426587.2:n.334-10C=
XR_946532.1:n.334-10C=
XM_005270412.4:c.255-10C= XP_005270469.1:n.255-10C=
XM_005270413.5:c.99-10C= XP_005270470.1:n.99-10C=
XM_011540569.3:c.-49+120C= XP_011538871.1:n.-49+120C=
XM_024452837.1:c.186-10C= XP_024308605.1:n.186-10C=
XR_001736951.2:n.424-10C=
XR_002959287.1:n.826-10C=
XR_246230.4:n.424-10C=
XR_426587.4:n.334-10C=
XR_946532.3:n.334-10C=
NM_025077.4:c.237-10C= MANE Select NP_079353.3:n.237-10C=