Canonical Allele Identifier: CA2246175734
Gene: CTC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8232130_8232131delinsTG , CM000679.2:g.8232130_8232131delinsTG GRCh38
NC_000017.10:g.8135448_8135449delinsTG , CM000679.1:g.8135448_8135449delinsTG GRCh37
NC_000017.9:g.8076173_8076174delinsTG NCBI36
NG_032148.1:g.20965_20966delinsCA
NG_032148.2:g.20965_20966delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000580299.2:c.2157_2158delinsCA ENSP00000462607.2:p.Pro719=
ENST00000581729.2:c.2157_2158delinsCA ENSP00000462720.2:p.Pro719=
ENST00000581967.2:n.2609_2610delinsCA
ENST00000583254.2:n.2863_2864delinsCA
ENST00000699849.1:c.1260_1261delinsCA ENSP00000514647.1:p.Pro420=
ENST00000699850.1:n.1420_1421delinsCA
ENST00000699851.1:n.2179_2180delinsCA
ENST00000699852.1:c.*833_*834delinsCA ENSP00000514648.1:n.*833_*834delinsCA
ENST00000699853.1:c.2157_2158delinsCA ENSP00000514649.1:p.Pro719=
ENST00000699854.1:n.1950_1951delinsCA
ENST00000699855.1:n.2609_2610delinsCA
ENST00000699856.1:c.2157_2158delinsCA ENSP00000514650.1:p.Pro719=
ENST00000699857.1:n.2165_2166delinsCA
ENST00000699858.1:c.*770_*771delinsCA ENSP00000514651.1:n.*770_*771delinsCA
ENST00000699859.1:c.2028_2029delinsCA ENSP00000514652.1:p.Pro676=
ENST00000699860.1:n.263_264delinsCA
ENST00000699861.1:n.2179_2180delinsCA
ENST00000699862.1:n.3117_3118delinsCA
ENST00000449476.7:c.2052_2053delinsCA ENSP00000396018.2:p.Pro684=
ENST00000581671.2:n.2146_2147delinsCA
ENST00000643543.1:c.*864_*865delinsCA ENSP00000494323.1:n.*864_*865delinsCA
ENST00000651323.1:c.2157_2158delinsCA MANE Select ENSP00000498499.1:p.Pro719=
ENST00000315684.12:c.2157_2158delinsCA ENSP00000313759.8:p.Pro719=
ENST00000449476.6:c.2052_2053delinsCA ENSP00000396018.2:p.Pro684=
ENST00000578240.1:n.385_386delinsCA
ENST00000578537.1:c.53_54delinsCA
NM_025099.5:c.2157_2158delinsCA NP_079375.3:p.Pro719=
NR_046431.1:n.2111_2112delinsCA
XM_006721577.2:c.2028_2029delinsCA XP_006721640.1:p.Pro676=
XM_006721578.2:c.2157_2158delinsCA XP_006721641.1:p.Pro719=
XM_006721579.2:c.2157_2158delinsCA XP_006721642.1:p.Pro719=
XM_011524010.1:c.2052_2053delinsCA XP_011522312.1:p.Pro684=
XM_011524011.1:c.1260_1261delinsCA XP_011522313.1:p.Pro420=
XR_429823.2:n.2200_2201delinsCA
XR_429824.2:n.2200_2201delinsCA
XR_429825.1:n.2200_2201delinsCA
NM_025099.6:c.2157_2158delinsCA MANE Select NP_079375.3:p.Pro719=
XM_006721577.3:c.2028_2029delinsCA XP_006721640.1:p.Pro676=
XM_006721578.3:c.2157_2158delinsCA XP_006721641.1:p.Pro719=
XM_011524010.2:c.2052_2053delinsCA XP_011522312.1:p.Pro684=
XM_011524011.2:c.1260_1261delinsCA XP_011522313.1:p.Pro420=
XR_001752639.1:n.2071_2072delinsCA
XR_001752640.1:n.2200_2201delinsCA
XR_001752641.1:n.2200_2201delinsCA
XR_001752642.1:n.2200_2201delinsCA
XR_001752643.1:n.2630_2631delinsCA
XR_002958073.1:n.2200_2201delinsCA
XR_429823.3:n.2200_2201delinsCA
XR_429824.3:n.2200_2201delinsCA
NR_046431.2:n.2072_2073delinsCA