Canonical Allele Identifier: CA1001248896

Linked Data

dbSNP Id: rs1646901838
gnomAD v3: 1-45340814-T-C
gnomAD v4: 1-45340814-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45340814T>C , CM000663.2:g.45340814T>C GRCh38
NC_000001.10:g.45806486T>C , CM000663.1:g.45806486T>C GRCh37
NC_000001.9:g.45579073T>C NCBI36
NG_008189.1:g.4657A>G , LRG_220:g.4657A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000372090.6:c.53-259T>C (TOE1) MANE Select ENSP00000361162.5:n.53-259T>C
ENST00000671898.1:c.541-6303A>G ENSP00000499896.1:n.541-6303A>G
ENST00000672011.1:c.-560A>G (MUTYH) ENSP00000500418.1:n.-560A>G
ENST00000372090.5:c.53-259T>C (TOE1) ENSP00000361162.5:n.53-259T>C
ENST00000471337.5:n.131-259T>C (TOE1)
ENST00000477731.5:n.272-259T>C (TOE1)
ENST00000495703.5:n.323-259T>C (TOE1)
NM_025077.3:c.53-259T>C (TOE1) NP_079353.3:n.53-259T>C
XM_005270412.2:c.71-259T>C (TOE1) XP_005270469.1:n.71-259T>C
XM_005270413.3:c.-86-259T>C (TOE1) XP_005270470.1:n.-86-259T>C
XM_011540569.1:c.-232-259T>C (TOE1) XP_011538871.1:n.-232-259T>C
XR_246230.2:n.330-259T>C (TOE1)
XR_426587.2:n.150-259T>C (TOE1)
XR_946532.1:n.150-259T>C (TOE1)
XM_005270412.4:c.71-259T>C (TOE1) XP_005270469.1:n.71-259T>C
XM_005270413.5:c.-86-259T>C (TOE1) XP_005270470.1:n.-86-259T>C
XM_011540569.3:c.-232-259T>C (TOE1) XP_011538871.1:n.-232-259T>C
XM_024452837.1:c.-86-259T>C (TOE1) XP_024308605.1:n.-86-259T>C
XR_001736951.2:n.240-259T>C (TOE1)
XR_002959287.1:n.555-259T>C (TOE1)
XR_246230.4:n.240-259T>C (TOE1)
XR_426587.4:n.150-259T>C (TOE1)
XR_946532.3:n.150-259T>C (TOE1)
NM_025077.4:c.53-259T>C (TOE1) MANE Select NP_079353.3:n.53-259T>C