Canonical Allele Identifier: CA2581663958

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45340760C>G , CM000663.2:g.45340760C>G GRCh38
NC_000001.10:g.45806432C>G , CM000663.1:g.45806432C>G GRCh37
NC_000001.9:g.45579019C>G NCBI36
NG_008189.1:g.4711G>C , LRG_220:g.4711G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000372090.6:c.53-313C>G (TOE1) MANE Select ENSP00000361162.5:n.53-313C>G
ENST00000671898.1:c.541-6249G>C ENSP00000499896.1:n.541-6249G>C
ENST00000672011.1:c.-506G>C (MUTYH) ENSP00000500418.1:n.-506G>C
ENST00000372090.5:c.53-313C>G (TOE1) ENSP00000361162.5:n.53-313C>G
ENST00000471337.5:n.131-313C>G (TOE1)
ENST00000477731.5:n.272-313C>G (TOE1)
ENST00000495703.5:n.322+218C>G (TOE1)
NM_025077.3:c.53-313C>G (TOE1) NP_079353.3:n.53-313C>G
XM_005270412.2:c.71-313C>G (TOE1) XP_005270469.1:n.71-313C>G
XM_005270413.3:c.-87+218C>G (TOE1) XP_005270470.1:n.-87+218C>G
XM_011540569.1:c.-232-313C>G (TOE1) XP_011538871.1:n.-232-313C>G
XR_246230.2:n.330-313C>G (TOE1)
XR_426587.2:n.150-313C>G (TOE1)
XR_946532.1:n.150-313C>G (TOE1)
XM_005270412.4:c.71-313C>G (TOE1) XP_005270469.1:n.71-313C>G
XM_005270413.5:c.-87+218C>G (TOE1) XP_005270470.1:n.-87+218C>G
XM_011540569.3:c.-232-313C>G (TOE1) XP_011538871.1:n.-232-313C>G
XM_024452837.1:c.-87+218C>G (TOE1) XP_024308605.1:n.-87+218C>G
XR_001736951.2:n.240-313C>G (TOE1)
XR_002959287.1:n.555-313C>G (TOE1)
XR_246230.4:n.240-313C>G (TOE1)
XR_426587.4:n.150-313C>G (TOE1)
XR_946532.3:n.150-313C>G (TOE1)
NM_025077.4:c.53-313C>G (TOE1) MANE Select NP_079353.3:n.53-313C>G