Canonical Allele Identifier: CA2645383605

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45340592_45340593insA , CM000663.2:g.45340592_45340593insA GRCh38
NC_000001.10:g.45806264_45806265insA , CM000663.1:g.45806264_45806265insA GRCh37
NC_000001.9:g.45578851_45578852insA NCBI36
NG_008189.1:g.4878_4879insT , LRG_220:g.4878_4879insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000372090.6:c.52+288_52+289insA (TOE1) MANE Select ENSP00000361162.5:n.52+288_52+289insA
ENST00000671898.1:c.541-6082_541-6081insT ENSP00000499896.1:n.541-6082_541-6081insT
ENST00000672011.1:c.-339_-338insT (MUTYH) ENSP00000500418.1:n.-339_-338insT
ENST00000372090.5:c.52+288_52+289insA (TOE1) ENSP00000361162.5:n.52+288_52+289insA
ENST00000471337.5:n.130+288_130+289insA (TOE1)
ENST00000477731.5:n.271+270_271+271insA (TOE1)
ENST00000495703.5:n.322+50_322+51insA (TOE1)
NM_025077.3:c.52+288_52+289insA (TOE1) NP_079353.3:n.52+288_52+289insA
XM_005270412.2:c.70+270_70+271insA (TOE1) XP_005270469.1:n.70+270_70+271insA
XM_005270413.3:c.-87+50_-87+51insA (TOE1) XP_005270470.1:n.-87+50_-87+51insA
XM_011540569.1:c.-233+288_-233+289insA (TOE1) XP_011538871.1:n.-233+288_-233+289insA
XR_246230.2:n.329+288_329+289insA (TOE1)
XR_426587.2:n.149+270_149+271insA (TOE1)
XR_946532.1:n.149+270_149+271insA (TOE1)
XM_005270412.4:c.70+270_70+271insA (TOE1) XP_005270469.1:n.70+270_70+271insA
XM_005270413.5:c.-87+50_-87+51insA (TOE1) XP_005270470.1:n.-87+50_-87+51insA
XM_011540569.3:c.-233+288_-233+289insA (TOE1) XP_011538871.1:n.-233+288_-233+289insA
XM_024452837.1:c.-87+50_-87+51insA (TOE1) XP_024308605.1:n.-87+50_-87+51insA
XR_001736951.2:n.239+288_239+289insA (TOE1)
XR_002959287.1:n.554+288_554+289insA (TOE1)
XR_246230.4:n.239+288_239+289insA (TOE1)
XR_426587.4:n.149+270_149+271insA (TOE1)
XR_946532.3:n.149+270_149+271insA (TOE1)
NM_025077.4:c.52+288_52+289insA (TOE1) MANE Select NP_079353.3:n.52+288_52+289insA