Canonical Allele Identifier: CA2473716492

Linked Data

dbSNP Id: rs1646899307

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45340793_45340795del , CM000663.2:g.45340793_45340795del GRCh38
NC_000001.10:g.45806465_45806467del , CM000663.1:g.45806465_45806467del GRCh37
NC_000001.9:g.45579052_45579054del NCBI36
NG_008189.1:g.4679_4681del , LRG_220:g.4679_4681del

Transcript Alleles

HGVS Amino-acid change
ENST00000372090.6:c.53-280_53-278del (TOE1) MANE Select ENSP00000361162.5:n.53-280_53-278del
ENST00000671898.1:c.541-6281_541-6279del ENSP00000499896.1:n.541-6281_541-6279del
ENST00000672011.1:c.-538_-536del (MUTYH) ENSP00000500418.1:n.-538_-536del
ENST00000372090.5:c.53-280_53-278del (TOE1) ENSP00000361162.5:n.53-280_53-278del
ENST00000471337.5:n.131-280_131-278del (TOE1)
ENST00000477731.5:n.272-280_272-278del (TOE1)
ENST00000495703.5:n.322+251_322+253del (TOE1)
NM_025077.3:c.53-280_53-278del (TOE1) NP_079353.3:n.53-280_53-278del
XM_005270412.2:c.71-280_71-278del (TOE1) XP_005270469.1:n.71-280_71-278del
XM_005270413.3:c.-87+251_-87+253del (TOE1) XP_005270470.1:n.-87+251_-87+253del
XM_011540569.1:c.-232-280_-232-278del (TOE1) XP_011538871.1:n.-232-280_-232-278del
XR_246230.2:n.330-280_330-278del (TOE1)
XR_426587.2:n.150-280_150-278del (TOE1)
XR_946532.1:n.150-280_150-278del (TOE1)
XM_005270412.4:c.71-280_71-278del (TOE1) XP_005270469.1:n.71-280_71-278del
XM_005270413.5:c.-87+251_-87+253del (TOE1) XP_005270470.1:n.-87+251_-87+253del
XM_011540569.3:c.-232-280_-232-278del (TOE1) XP_011538871.1:n.-232-280_-232-278del
XM_024452837.1:c.-87+251_-87+253del (TOE1) XP_024308605.1:n.-87+251_-87+253del
XR_001736951.2:n.240-280_240-278del (TOE1)
XR_002959287.1:n.555-280_555-278del (TOE1)
XR_246230.4:n.240-280_240-278del (TOE1)
XR_426587.4:n.150-280_150-278del (TOE1)
XR_946532.3:n.150-280_150-278del (TOE1)
NM_025077.4:c.53-280_53-278del (TOE1) MANE Select NP_079353.3:n.53-280_53-278del