Canonical Allele Identifier: CA2246175762
Gene: CTC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8232136C= , CM000679.2:g.8232136C= GRCh38
NC_000017.10:g.8135454C= , CM000679.1:g.8135454C= GRCh37
NC_000017.9:g.8076179C= NCBI36
NG_032148.1:g.20960G=
NG_032148.2:g.20960G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000580299.2:c.2152G= ENSP00000462607.2:p.Asp718=
ENST00000581729.2:c.2152G= ENSP00000462720.2:p.Asp718=
ENST00000581967.2:n.2604G=
ENST00000583254.2:n.2858G=
ENST00000699849.1:c.1255G= ENSP00000514647.1:p.Asp419=
ENST00000699850.1:n.1415G=
ENST00000699851.1:n.2174G=
ENST00000699852.1:c.*828G= ENSP00000514648.1:n.*828G=
ENST00000699853.1:c.2152G= ENSP00000514649.1:p.Asp718=
ENST00000699854.1:n.1945G=
ENST00000699855.1:n.2604G=
ENST00000699856.1:c.2152G= ENSP00000514650.1:p.Asp718=
ENST00000699857.1:n.2160G=
ENST00000699858.1:c.*765G= ENSP00000514651.1:n.*765G=
ENST00000699859.1:c.2023G= ENSP00000514652.1:p.Asp675=
ENST00000699860.1:n.258G=
ENST00000699861.1:n.2174G=
ENST00000699862.1:n.3112G=
ENST00000449476.7:c.2047G= ENSP00000396018.2:p.Asp683=
ENST00000581671.2:n.2141G=
ENST00000643543.1:c.*859G= ENSP00000494323.1:n.*859G=
ENST00000651323.1:c.2152G= MANE Select ENSP00000498499.1:p.Asp718=
ENST00000315684.12:c.2152G= ENSP00000313759.8:p.Asp718=
ENST00000449476.6:c.2047G= ENSP00000396018.2:p.Asp683=
ENST00000578240.1:n.380G=
ENST00000578537.1:c.48G=
NM_025099.5:c.2152G= NP_079375.3:p.Asp718=
NR_046431.1:n.2106G=
XM_006721577.2:c.2023G= XP_006721640.1:p.Asp675=
XM_006721578.2:c.2152G= XP_006721641.1:p.Asp718=
XM_006721579.2:c.2152G= XP_006721642.1:p.Asp718=
XM_011524010.1:c.2047G= XP_011522312.1:p.Asp683=
XM_011524011.1:c.1255G= XP_011522313.1:p.Asp419=
XR_429823.2:n.2195G=
XR_429824.2:n.2195G=
XR_429825.1:n.2195G=
NM_025099.6:c.2152G= MANE Select NP_079375.3:p.Asp718=
XM_006721577.3:c.2023G= XP_006721640.1:p.Asp675=
XM_006721578.3:c.2152G= XP_006721641.1:p.Asp718=
XM_011524010.2:c.2047G= XP_011522312.1:p.Asp683=
XM_011524011.2:c.1255G= XP_011522313.1:p.Asp419=
XR_001752639.1:n.2066G=
XR_001752640.1:n.2195G=
XR_001752641.1:n.2195G=
XR_001752642.1:n.2195G=
XR_001752643.1:n.2625G=
XR_002958073.1:n.2195G=
XR_429823.3:n.2195G=
XR_429824.3:n.2195G=
NR_046431.2:n.2067G=