Canonical Allele Identifier: CA2635985468
Gene: CTC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8232091_8232093del , CM000679.2:g.8232091_8232093del GRCh38
NC_000017.10:g.8135409_8135411del , CM000679.1:g.8135409_8135411del GRCh37
NC_000017.9:g.8076134_8076136del NCBI36
NG_032148.1:g.21007_21009del
NG_032148.2:g.21007_21009del

Transcript Alleles

HGVS Amino-acid Change
ENST00000580299.2:c.2199_2201del ENSP00000462607.2:p.Phe733del
ENST00000581729.2:c.2199_2201del ENSP00000462720.2:p.Phe733del
ENST00000581967.2:n.2651_2653del
ENST00000583254.2:n.2905_2907del
ENST00000699849.1:c.1302_1304del ENSP00000514647.1:p.Phe434del
ENST00000699850.1:n.1462_1464del
ENST00000699851.1:n.2221_2223del
ENST00000699852.1:c.*875_*877del ENSP00000514648.1:n.*875_*877del
ENST00000699853.1:c.2199_2201del ENSP00000514649.1:p.Phe733del
ENST00000699854.1:n.1992_1994del
ENST00000699855.1:n.2651_2653del
ENST00000699856.1:c.2199_2201del ENSP00000514650.1:p.Phe733del
ENST00000699857.1:n.2207_2209del
ENST00000699858.1:c.*812_*814del ENSP00000514651.1:n.*812_*814del
ENST00000699859.1:c.2070_2072del ENSP00000514652.1:p.Phe690del
ENST00000699860.1:n.305_307del
ENST00000699861.1:n.2221_2223del
ENST00000699862.1:n.3159_3161del
ENST00000449476.7:c.2094_2096del ENSP00000396018.2:p.Phe698del
ENST00000581671.2:n.2188_2190del
ENST00000643543.1:c.*906_*908del ENSP00000494323.1:n.*906_*908del
ENST00000651323.1:c.2199_2201del MANE Select ENSP00000498499.1:p.Phe733del
ENST00000315684.12:c.2199_2201del ENSP00000313759.8:p.Phe733del
ENST00000449476.6:c.2094_2096del ENSP00000396018.2:p.Phe698del
ENST00000578240.1:n.427_429del
ENST00000578537.1:c.95_97del
NM_025099.5:c.2199_2201del NP_079375.3:p.Phe733del
NR_046431.1:n.2153_2155del
XM_006721577.2:c.2070_2072del XP_006721640.1:p.Phe690del
XM_006721578.2:c.2199_2201del XP_006721641.1:p.Phe733del
XM_006721579.2:c.2199_2201del XP_006721642.1:p.Phe733del
XM_011524010.1:c.2094_2096del XP_011522312.1:p.Phe698del
XM_011524011.1:c.1302_1304del XP_011522313.1:p.Phe434del
XR_429823.2:n.2242_2244del
XR_429824.2:n.2242_2244del
XR_429825.1:n.2242_2244del
NM_025099.6:c.2199_2201del MANE Select NP_079375.3:p.Phe733del
XM_006721577.3:c.2070_2072del XP_006721640.1:p.Phe690del
XM_006721578.3:c.2199_2201del XP_006721641.1:p.Phe733del
XM_011524010.2:c.2094_2096del XP_011522312.1:p.Phe698del
XM_011524011.2:c.1302_1304del XP_011522313.1:p.Phe434del
XR_001752639.1:n.2113_2115del
XR_001752640.1:n.2242_2244del
XR_001752641.1:n.2242_2244del
XR_001752642.1:n.2242_2244del
XR_001752643.1:n.2672_2674del
XR_002958073.1:n.2242_2244del
XR_429823.3:n.2242_2244del
XR_429824.3:n.2242_2244del
NR_046431.2:n.2114_2116del