Canonical Allele Identifier: CA2645383546

Linked Data

gnomAD v4: 1-45340493-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45340493C>T , CM000663.2:g.45340493C>T GRCh38
NC_000001.10:g.45806165C>T , CM000663.1:g.45806165C>T GRCh37
NC_000001.9:g.45578752C>T NCBI36
NG_008189.1:g.4978G>A , LRG_220:g.4978G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000372090.6:c.52+189C>T (TOE1) MANE Select ENSP00000361162.5:n.52+189C>T
ENST00000671898.1:c.541-5982G>A ENSP00000499896.1:n.541-5982G>A
ENST00000672011.1:c.-239G>A (MUTYH) ENSP00000500418.1:n.-239G>A
ENST00000372090.5:c.52+189C>T (TOE1) ENSP00000361162.5:n.52+189C>T
ENST00000471337.5:n.130+189C>T (TOE1)
ENST00000477731.5:n.271+171C>T (TOE1)
ENST00000495703.5:n.273C>T (TOE1)
NM_025077.3:c.52+189C>T (TOE1) NP_079353.3:n.52+189C>T
XM_005270412.2:c.70+171C>T (TOE1) XP_005270469.1:n.70+171C>T
XM_005270413.3:c.-136C>T (TOE1) XP_005270470.1:n.-136C>T
XM_011540569.1:c.-233+189C>T (TOE1) XP_011538871.1:n.-233+189C>T
XR_246230.2:n.329+189C>T (TOE1)
XR_426587.2:n.149+171C>T (TOE1)
XR_946532.1:n.149+171C>T (TOE1)
XM_005270412.4:c.70+171C>T (TOE1) XP_005270469.1:n.70+171C>T
XM_005270413.5:c.-136C>T (TOE1) XP_005270470.1:n.-136C>T
XM_011540569.3:c.-233+189C>T (TOE1) XP_011538871.1:n.-233+189C>T
XM_024452837.1:c.-136C>T (TOE1) XP_024308605.1:n.-136C>T
XR_001736951.2:n.239+189C>T (TOE1)
XR_002959287.1:n.554+189C>T (TOE1)
XR_246230.4:n.239+189C>T (TOE1)
XR_426587.4:n.149+171C>T (TOE1)
XR_946532.3:n.149+171C>T (TOE1)
NM_025077.4:c.52+189C>T (TOE1) MANE Select NP_079353.3:n.52+189C>T