Canonical Allele Identifier: CA1146939316

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45340702G= , CM000663.2:g.45340702G= GRCh38
NC_000001.10:g.45806374G= , CM000663.1:g.45806374G= GRCh37
NC_000001.9:g.45578961G= NCBI36
NG_008189.1:g.4769C= , LRG_220:g.4769C=

Transcript Alleles

HGVS Amino-acid change
ENST00000372090.6:c.53-371G= (TOE1) MANE Select ENSP00000361162.5:n.53-371G=
ENST00000671898.1:c.541-6191C= ENSP00000499896.1:n.541-6191C=
ENST00000672011.1:c.-448C= (MUTYH) ENSP00000500418.1:n.-448C=
ENST00000372090.5:c.53-371G= (TOE1) ENSP00000361162.5:n.53-371G=
ENST00000471337.5:n.131-371G= (TOE1)
ENST00000477731.5:n.272-371G= (TOE1)
ENST00000495703.5:n.322+160G= (TOE1)
NM_025077.3:c.53-371G= (TOE1) NP_079353.3:n.53-371G=
XM_005270412.2:c.71-371G= (TOE1) XP_005270469.1:n.71-371G=
XM_005270413.3:c.-87+160G= (TOE1) XP_005270470.1:n.-87+160G=
XM_011540569.1:c.-232-371G= (TOE1) XP_011538871.1:n.-232-371G=
XR_246230.2:n.330-371G= (TOE1)
XR_426587.2:n.150-371G= (TOE1)
XR_946532.1:n.150-371G= (TOE1)
XM_005270412.4:c.71-371G= (TOE1) XP_005270469.1:n.71-371G=
XM_005270413.5:c.-87+160G= (TOE1) XP_005270470.1:n.-87+160G=
XM_011540569.3:c.-232-371G= (TOE1) XP_011538871.1:n.-232-371G=
XM_024452837.1:c.-87+160G= (TOE1) XP_024308605.1:n.-87+160G=
XR_001736951.2:n.240-371G= (TOE1)
XR_002959287.1:n.555-371G= (TOE1)
XR_246230.4:n.240-371G= (TOE1)
XR_426587.4:n.150-371G= (TOE1)
XR_946532.3:n.150-371G= (TOE1)
NM_025077.4:c.53-371G= (TOE1) MANE Select NP_079353.3:n.53-371G=