Canonical Allele Identifier: CA21847802

Linked Data

dbSNP Id: rs752084702

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45340888_45340889del , CM000663.2:g.45340888_45340889del GRCh38
NC_000001.10:g.45806560_45806561del , CM000663.1:g.45806560_45806561del GRCh37
NC_000001.9:g.45579147_45579148del NCBI36
NG_008189.1:g.4585_4586del , LRG_220:g.4585_4586del

Transcript Alleles

HGVS Amino-acid change
ENST00000372090.6:c.53-185_53-184del (TOE1) MANE Select ENSP00000361162.5:n.53-185_53-184del
ENST00000671898.1:c.541-6375_541-6374del ENSP00000499896.1:n.541-6375_541-6374del
ENST00000672011.1:c.-632_-631del (MUTYH) ENSP00000500418.1:n.-632_-631del
ENST00000372090.5:c.53-185_53-184del (TOE1) ENSP00000361162.5:n.53-185_53-184del
ENST00000471337.5:n.131-185_131-184del (TOE1)
ENST00000477731.5:n.272-185_272-184del (TOE1)
ENST00000495703.5:n.323-185_323-184del (TOE1)
NM_025077.3:c.53-185_53-184del (TOE1) NP_079353.3:n.53-185_53-184del
XM_005270412.2:c.71-185_71-184del (TOE1) XP_005270469.1:n.71-185_71-184del
XM_005270413.3:c.-86-185_-86-184del (TOE1) XP_005270470.1:n.-86-185_-86-184del
XM_011540569.1:c.-232-185_-232-184del (TOE1) XP_011538871.1:n.-232-185_-232-184del
XR_246230.2:n.330-185_330-184del (TOE1)
XR_426587.2:n.150-185_150-184del (TOE1)
XR_946532.1:n.150-185_150-184del (TOE1)
XM_005270412.4:c.71-185_71-184del (TOE1) XP_005270469.1:n.71-185_71-184del
XM_005270413.5:c.-86-185_-86-184del (TOE1) XP_005270470.1:n.-86-185_-86-184del
XM_011540569.3:c.-232-185_-232-184del (TOE1) XP_011538871.1:n.-232-185_-232-184del
XM_024452837.1:c.-86-185_-86-184del (TOE1) XP_024308605.1:n.-86-185_-86-184del
XR_001736951.2:n.240-185_240-184del (TOE1)
XR_002959287.1:n.555-185_555-184del (TOE1)
XR_246230.4:n.240-185_240-184del (TOE1)
XR_426587.4:n.150-185_150-184del (TOE1)
XR_946532.3:n.150-185_150-184del (TOE1)
NM_025077.4:c.53-185_53-184del (TOE1) MANE Select NP_079353.3:n.53-185_53-184del