Canonical Allele Identifier: CA2246175676
Gene: CTC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8232111_8232112delinsTG , CM000679.2:g.8232111_8232112delinsTG GRCh38
NC_000017.10:g.8135429_8135430delinsTG , CM000679.1:g.8135429_8135430delinsTG GRCh37
NC_000017.9:g.8076154_8076155delinsTG NCBI36
NG_032148.1:g.20984_20985delinsCA
NG_032148.2:g.20984_20985delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000580299.2:c.2176_2177delinsCA ENSP00000462607.2:p.His726=
ENST00000581729.2:c.2176_2177delinsCA ENSP00000462720.2:p.His726=
ENST00000581967.2:n.2628_2629delinsCA
ENST00000583254.2:n.2882_2883delinsCA
ENST00000699849.1:c.1279_1280delinsCA ENSP00000514647.1:p.His427=
ENST00000699850.1:n.1439_1440delinsCA
ENST00000699851.1:n.2198_2199delinsCA
ENST00000699852.1:c.*852_*853delinsCA ENSP00000514648.1:n.*852_*853delinsCA
ENST00000699853.1:c.2176_2177delinsCA ENSP00000514649.1:p.His726=
ENST00000699854.1:n.1969_1970delinsCA
ENST00000699855.1:n.2628_2629delinsCA
ENST00000699856.1:c.2176_2177delinsCA ENSP00000514650.1:p.His726=
ENST00000699857.1:n.2184_2185delinsCA
ENST00000699858.1:c.*789_*790delinsCA ENSP00000514651.1:n.*789_*790delinsCA
ENST00000699859.1:c.2047_2048delinsCA ENSP00000514652.1:p.His683=
ENST00000699860.1:n.282_283delinsCA
ENST00000699861.1:n.2198_2199delinsCA
ENST00000699862.1:n.3136_3137delinsCA
ENST00000449476.7:c.2071_2072delinsCA ENSP00000396018.2:p.His691=
ENST00000581671.2:n.2165_2166delinsCA
ENST00000643543.1:c.*883_*884delinsCA ENSP00000494323.1:n.*883_*884delinsCA
ENST00000651323.1:c.2176_2177delinsCA MANE Select ENSP00000498499.1:p.His726=
ENST00000315684.12:c.2176_2177delinsCA ENSP00000313759.8:p.His726=
ENST00000449476.6:c.2071_2072delinsCA ENSP00000396018.2:p.His691=
ENST00000578240.1:n.404_405delinsCA
ENST00000578537.1:c.72_73delinsCA
NM_025099.5:c.2176_2177delinsCA NP_079375.3:p.His726=
NR_046431.1:n.2130_2131delinsCA
XM_006721577.2:c.2047_2048delinsCA XP_006721640.1:p.His683=
XM_006721578.2:c.2176_2177delinsCA XP_006721641.1:p.His726=
XM_006721579.2:c.2176_2177delinsCA XP_006721642.1:p.His726=
XM_011524010.1:c.2071_2072delinsCA XP_011522312.1:p.His691=
XM_011524011.1:c.1279_1280delinsCA XP_011522313.1:p.His427=
XR_429823.2:n.2219_2220delinsCA
XR_429824.2:n.2219_2220delinsCA
XR_429825.1:n.2219_2220delinsCA
NM_025099.6:c.2176_2177delinsCA MANE Select NP_079375.3:p.His726=
XM_006721577.3:c.2047_2048delinsCA XP_006721640.1:p.His683=
XM_006721578.3:c.2176_2177delinsCA XP_006721641.1:p.His726=
XM_011524010.2:c.2071_2072delinsCA XP_011522312.1:p.His691=
XM_011524011.2:c.1279_1280delinsCA XP_011522313.1:p.His427=
XR_001752639.1:n.2090_2091delinsCA
XR_001752640.1:n.2219_2220delinsCA
XR_001752641.1:n.2219_2220delinsCA
XR_001752642.1:n.2219_2220delinsCA
XR_001752643.1:n.2649_2650delinsCA
XR_002958073.1:n.2219_2220delinsCA
XR_429823.3:n.2219_2220delinsCA
XR_429824.3:n.2219_2220delinsCA
NR_046431.2:n.2091_2092delinsCA