Canonical Allele Identifier: CA2473716527

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45340884_45340886delinsCCT , CM000663.2:g.45340884_45340886delinsCCT GRCh38
NC_000001.10:g.45806556_45806558delinsCCT , CM000663.1:g.45806556_45806558delinsCCT GRCh37
NC_000001.9:g.45579143_45579145delinsCCT NCBI36
NG_008189.1:g.4585_4587delinsAGG , LRG_220:g.4585_4587delinsAGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000372090.6:c.53-189_53-187delinsCCT (TOE1) MANE Select ENSP00000361162.5:n.53-189_53-187delinsCCT
ENST00000671898.1:c.541-6375_541-6373delinsAGG ENSP00000499896.1:n.541-6375_541-6373delinsAGG
ENST00000672011.1:c.-632_-630delinsAGG (MUTYH) ENSP00000500418.1:n.-632_-630delinsAGG
ENST00000372090.5:c.53-189_53-187delinsCCT (TOE1) ENSP00000361162.5:n.53-189_53-187delinsCCT
ENST00000471337.5:n.131-189_131-187delinsCCT (TOE1)
ENST00000477731.5:n.272-189_272-187delinsCCT (TOE1)
ENST00000495703.5:n.323-189_323-187delinsCCT (TOE1)
NM_025077.3:c.53-189_53-187delinsCCT (TOE1) NP_079353.3:n.53-189_53-187delinsCCT
XM_005270412.2:c.71-189_71-187delinsCCT (TOE1) XP_005270469.1:n.71-189_71-187delinsCCT
XM_005270413.3:c.-86-189_-86-187delinsCCT (TOE1) XP_005270470.1:n.-86-189_-86-187delinsCCT
XM_011540569.1:c.-232-189_-232-187delinsCCT (TOE1) XP_011538871.1:n.-232-189_-232-187delinsCCT
XR_246230.2:n.330-189_330-187delinsCCT (TOE1)
XR_426587.2:n.150-189_150-187delinsCCT (TOE1)
XR_946532.1:n.150-189_150-187delinsCCT (TOE1)
XM_005270412.4:c.71-189_71-187delinsCCT (TOE1) XP_005270469.1:n.71-189_71-187delinsCCT
XM_005270413.5:c.-86-189_-86-187delinsCCT (TOE1) XP_005270470.1:n.-86-189_-86-187delinsCCT
XM_011540569.3:c.-232-189_-232-187delinsCCT (TOE1) XP_011538871.1:n.-232-189_-232-187delinsCCT
XM_024452837.1:c.-86-189_-86-187delinsCCT (TOE1) XP_024308605.1:n.-86-189_-86-187delinsCCT
XR_001736951.2:n.240-189_240-187delinsCCT (TOE1)
XR_002959287.1:n.555-189_555-187delinsCCT (TOE1)
XR_246230.4:n.240-189_240-187delinsCCT (TOE1)
XR_426587.4:n.150-189_150-187delinsCCT (TOE1)
XR_946532.3:n.150-189_150-187delinsCCT (TOE1)
NM_025077.4:c.53-189_53-187delinsCCT (TOE1) MANE Select NP_079353.3:n.53-189_53-187delinsCCT