Canonical Allele Identifier: CA2246188630
Gene: CTC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8230964C= , CM000679.2:g.8230964C= GRCh38
NC_000017.10:g.8134282C= , CM000679.1:g.8134282C= GRCh37
NC_000017.9:g.8075007C= NCBI36
NG_032148.1:g.22132G=
NG_032148.2:g.22132G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000580299.2:c.2670-313G= ENSP00000462607.2:n.2670-313G=
ENST00000581729.2:c.2670-313G= ENSP00000462720.2:n.2670-313G=
ENST00000581967.2:n.3122-313G=
ENST00000583254.2:n.4030G=
ENST00000699849.1:c.1773-313G= ENSP00000514647.1:n.1773-313G=
ENST00000699850.1:n.1933-313G=
ENST00000699851.1:n.2692-313G=
ENST00000699852.1:c.*1346-313G= ENSP00000514648.1:n.*1346-313G=
ENST00000699853.1:c.2670-313G= ENSP00000514649.1:n.2670-313G=
ENST00000699854.1:n.2463-313G=
ENST00000699855.1:n.3122-313G=
ENST00000699856.1:c.2670-313G= ENSP00000514650.1:n.2670-313G=
ENST00000699857.1:n.2678-313G=
ENST00000699858.1:c.*1283-313G= ENSP00000514651.1:n.*1283-313G=
ENST00000699859.1:c.2541-313G= ENSP00000514652.1:n.2541-313G=
ENST00000699860.1:n.582-313G=
ENST00000699861.1:n.2692-313G=
ENST00000699862.1:n.3630-313G=
ENST00000449476.7:c.2565-313G= ENSP00000396018.2:n.2565-313G=
ENST00000581671.2:n.2659-313G=
ENST00000643543.1:c.*1377-313G= ENSP00000494323.1:n.*1377-313G=
ENST00000651323.1:c.2670-313G= MANE Select ENSP00000498499.1:n.2670-313G=
ENST00000315684.12:c.2670-313G= ENSP00000313759.8:n.2670-313G=
ENST00000449476.6:c.2565-313G= ENSP00000396018.2:n.2565-313G=
ENST00000578240.1:n.898-313G=
ENST00000578441.5:n.171-313G=
ENST00000578537.1:c.372-313G=
NM_025099.5:c.2670-313G= NP_079375.3:n.2670-313G=
NR_046431.1:n.2624-313G=
XM_006721577.2:c.2541-313G= XP_006721640.1:n.2541-313G=
XM_006721578.2:c.2670-313G= XP_006721641.1:n.2670-313G=
XM_006721579.2:c.2670-313G= XP_006721642.1:n.2670-313G=
XM_011524010.1:c.2565-313G= XP_011522312.1:n.2565-313G=
XM_011524011.1:c.1773-313G= XP_011522313.1:n.1773-313G=
XR_429823.2:n.2713-313G=
XR_429824.2:n.2713-313G=
XR_429825.1:n.2519-313G=
NM_025099.6:c.2670-313G= MANE Select NP_079375.3:n.2670-313G=
XM_006721577.3:c.2541-313G= XP_006721640.1:n.2541-313G=
XM_006721578.3:c.2670-313G= XP_006721641.1:n.2670-313G=
XM_011524010.2:c.2565-313G= XP_011522312.1:n.2565-313G=
XM_011524011.2:c.1773-313G= XP_011522313.1:n.1773-313G=
XR_001752639.1:n.2584-313G=
XR_001752640.1:n.2713-313G=
XR_001752641.1:n.2713-313G=
XR_001752642.1:n.2519-313G=
XR_001752643.1:n.3143-313G=
XR_002958073.1:n.2519-313G=
XR_429823.3:n.2713-313G=
XR_429824.3:n.2713-313G=
NR_046431.2:n.2585-313G=