Canonical Allele Identifier: CA397978315
Gene: CTC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8232081C>T , CM000679.2:g.8232081C>T GRCh38
NC_000017.10:g.8135399C>T , CM000679.1:g.8135399C>T GRCh37
NC_000017.9:g.8076124C>T NCBI36
NG_032148.1:g.21015G>A
NG_032148.2:g.21015G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000580299.2:c.2207G>A ENSP00000462607.2:p.Cys736Tyr
ENST00000581729.2:c.2207G>A ENSP00000462720.2:p.Cys736Tyr
ENST00000581967.2:n.2659G>A
ENST00000583254.2:n.2913G>A
ENST00000699849.1:c.1310G>A ENSP00000514647.1:p.Cys437Tyr
ENST00000699850.1:n.1470G>A
ENST00000699851.1:n.2229G>A
ENST00000699852.1:c.*883G>A ENSP00000514648.1:n.*883G>A
ENST00000699853.1:c.2207G>A ENSP00000514649.1:p.Cys736Tyr
ENST00000699854.1:n.2000G>A
ENST00000699855.1:n.2659G>A
ENST00000699856.1:c.2207G>A ENSP00000514650.1:p.Cys736Tyr
ENST00000699857.1:n.2215G>A
ENST00000699858.1:c.*820G>A ENSP00000514651.1:n.*820G>A
ENST00000699859.1:c.2078G>A ENSP00000514652.1:p.Cys693Tyr
ENST00000699860.1:n.313G>A
ENST00000699861.1:n.2229G>A
ENST00000699862.1:n.3167G>A
ENST00000449476.7:c.2102G>A ENSP00000396018.2:p.Cys701Tyr
ENST00000581671.2:n.2196G>A
ENST00000643543.1:c.*914G>A ENSP00000494323.1:n.*914G>A
ENST00000651323.1:c.2207G>A MANE Select ENSP00000498499.1:p.Cys736Tyr
ENST00000315684.12:c.2207G>A ENSP00000313759.8:p.Cys736Tyr
ENST00000449476.6:c.2102G>A ENSP00000396018.2:p.Cys701Tyr
ENST00000578240.1:n.435G>A
ENST00000578537.1:c.103G>A
NM_025099.5:c.2207G>A NP_079375.3:p.Cys736Tyr
NR_046431.1:n.2161G>A
XM_006721577.2:c.2078G>A XP_006721640.1:p.Cys693Tyr
XM_006721578.2:c.2207G>A XP_006721641.1:p.Cys736Tyr
XM_006721579.2:c.2207G>A XP_006721642.1:p.Cys736Tyr
XM_011524010.1:c.2102G>A XP_011522312.1:p.Cys701Tyr
XM_011524011.1:c.1310G>A XP_011522313.1:p.Cys437Tyr
XR_429823.2:n.2250G>A
XR_429824.2:n.2250G>A
XR_429825.1:n.2250G>A
NM_025099.6:c.2207G>A MANE Select NP_079375.3:p.Cys736Tyr
XM_006721577.3:c.2078G>A XP_006721640.1:p.Cys693Tyr
XM_006721578.3:c.2207G>A XP_006721641.1:p.Cys736Tyr
XM_011524010.2:c.2102G>A XP_011522312.1:p.Cys701Tyr
XM_011524011.2:c.1310G>A XP_011522313.1:p.Cys437Tyr
XR_001752639.1:n.2121G>A
XR_001752640.1:n.2250G>A
XR_001752641.1:n.2250G>A
XR_001752642.1:n.2250G>A
XR_001752643.1:n.2680G>A
XR_002958073.1:n.2250G>A
XR_429823.3:n.2250G>A
XR_429824.3:n.2250G>A
NR_046431.2:n.2122G>A