Canonical Allele Identifier: CA2246189290
Gene: CTC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8231570G= , CM000679.2:g.8231570G= GRCh38
NC_000017.10:g.8134888G= , CM000679.1:g.8134888G= GRCh37
NC_000017.9:g.8075613G= NCBI36
NG_032148.1:g.21526C=
NG_032148.2:g.21526C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000580299.2:c.2476-101C= ENSP00000462607.2:n.2476-101C=
ENST00000581729.2:c.2476-101C= ENSP00000462720.2:n.2476-101C=
ENST00000581967.2:n.2928-101C=
ENST00000583254.2:n.3424C=
ENST00000699849.1:c.1579-101C= ENSP00000514647.1:n.1579-101C=
ENST00000699850.1:n.1739-101C=
ENST00000699851.1:n.2498-101C=
ENST00000699852.1:c.*1152-101C= ENSP00000514648.1:n.*1152-101C=
ENST00000699853.1:c.2476-101C= ENSP00000514649.1:n.2476-101C=
ENST00000699854.1:n.2269-101C=
ENST00000699855.1:n.2928-101C=
ENST00000699856.1:c.2476-101C= ENSP00000514650.1:n.2476-101C=
ENST00000699857.1:n.2484-101C=
ENST00000699858.1:c.*1089-101C= ENSP00000514651.1:n.*1089-101C=
ENST00000699859.1:c.2347-101C= ENSP00000514652.1:n.2347-101C=
ENST00000699860.1:n.581+156C=
ENST00000699861.1:n.2498-101C=
ENST00000699862.1:n.3436-101C=
ENST00000449476.7:c.2371-101C= ENSP00000396018.2:n.2371-101C=
ENST00000581671.2:n.2465-101C=
ENST00000643543.1:c.*1183-101C= ENSP00000494323.1:n.*1183-101C=
ENST00000651323.1:c.2476-101C= MANE Select ENSP00000498499.1:n.2476-101C=
ENST00000315684.12:c.2476-101C= ENSP00000313759.8:n.2476-101C=
ENST00000449476.6:c.2371-101C= ENSP00000396018.2:n.2371-101C=
ENST00000578240.1:n.704-101C=
ENST00000578537.1:c.371+156C=
NM_025099.5:c.2476-101C= NP_079375.3:n.2476-101C=
NR_046431.1:n.2430-101C=
XM_006721577.2:c.2347-101C= XP_006721640.1:n.2347-101C=
XM_006721578.2:c.2476-101C= XP_006721641.1:n.2476-101C=
XM_006721579.2:c.2476-101C= XP_006721642.1:n.2476-101C=
XM_011524010.1:c.2371-101C= XP_011522312.1:n.2371-101C=
XM_011524011.1:c.1579-101C= XP_011522313.1:n.1579-101C=
XR_429823.2:n.2519-101C=
XR_429824.2:n.2519-101C=
XR_429825.1:n.2518+156C=
NM_025099.6:c.2476-101C= MANE Select NP_079375.3:n.2476-101C=
XM_006721577.3:c.2347-101C= XP_006721640.1:n.2347-101C=
XM_006721578.3:c.2476-101C= XP_006721641.1:n.2476-101C=
XM_011524010.2:c.2371-101C= XP_011522312.1:n.2371-101C=
XM_011524011.2:c.1579-101C= XP_011522313.1:n.1579-101C=
XR_001752639.1:n.2390-101C=
XR_001752640.1:n.2519-101C=
XR_001752641.1:n.2519-101C=
XR_001752642.1:n.2518+156C=
XR_001752643.1:n.2949-101C=
XR_002958073.1:n.2518+156C=
XR_429823.3:n.2519-101C=
XR_429824.3:n.2519-101C=
NR_046431.2:n.2391-101C=