Canonical Allele Identifier: CA2522793969

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45340583T>G , CM000663.2:g.45340583T>G GRCh38
NC_000001.10:g.45806255T>G , CM000663.1:g.45806255T>G GRCh37
NC_000001.9:g.45578842T>G NCBI36
NG_008189.1:g.4888A>C , LRG_220:g.4888A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000372090.6:c.52+279T>G (TOE1) MANE Select ENSP00000361162.5:n.52+279T>G
ENST00000671898.1:c.541-6072A>C ENSP00000499896.1:n.541-6072A>C
ENST00000672011.1:c.-329A>C (MUTYH) ENSP00000500418.1:n.-329A>C
ENST00000372090.5:c.52+279T>G (TOE1) ENSP00000361162.5:n.52+279T>G
ENST00000471337.5:n.130+279T>G (TOE1)
ENST00000477731.5:n.271+261T>G (TOE1)
ENST00000495703.5:n.322+41T>G (TOE1)
NM_025077.3:c.52+279T>G (TOE1) NP_079353.3:n.52+279T>G
XM_005270412.2:c.70+261T>G (TOE1) XP_005270469.1:n.70+261T>G
XM_005270413.3:c.-87+41T>G (TOE1) XP_005270470.1:n.-87+41T>G
XM_011540569.1:c.-233+279T>G (TOE1) XP_011538871.1:n.-233+279T>G
XR_246230.2:n.329+279T>G (TOE1)
XR_426587.2:n.149+261T>G (TOE1)
XR_946532.1:n.149+261T>G (TOE1)
XM_005270412.4:c.70+261T>G (TOE1) XP_005270469.1:n.70+261T>G
XM_005270413.5:c.-87+41T>G (TOE1) XP_005270470.1:n.-87+41T>G
XM_011540569.3:c.-233+279T>G (TOE1) XP_011538871.1:n.-233+279T>G
XM_024452837.1:c.-87+41T>G (TOE1) XP_024308605.1:n.-87+41T>G
XR_001736951.2:n.239+279T>G (TOE1)
XR_002959287.1:n.554+279T>G (TOE1)
XR_246230.4:n.239+279T>G (TOE1)
XR_426587.4:n.149+261T>G (TOE1)
XR_946532.3:n.149+261T>G (TOE1)
NM_025077.4:c.52+279T>G (TOE1) MANE Select NP_079353.3:n.52+279T>G