Canonical Allele Identifier: CA497958749
Gene: CTC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.8135059T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8231741T>A , CM000679.2:g.8231741T>A GRCh38
NC_000017.10:g.8135059T>A , CM000679.1:g.8135059T>A GRCh37
NC_000017.9:g.8075784T>A NCBI36
NG_032148.1:g.21355A>T
NG_032148.2:g.21355A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000580299.2:c.2460A>T ENSP00000462607.2:p.Ile820=
ENST00000581729.2:c.2460A>T ENSP00000462720.2:p.Ile820=
ENST00000581967.2:n.2912A>T
ENST00000583254.2:n.3253A>T
ENST00000699849.1:c.1563A>T ENSP00000514647.1:p.Ile521=
ENST00000699850.1:n.1723A>T
ENST00000699851.1:n.2482A>T
ENST00000699852.1:c.*1136A>T ENSP00000514648.1:n.*1136A>T
ENST00000699853.1:c.2460A>T ENSP00000514649.1:p.Ile820=
ENST00000699854.1:n.2253A>T
ENST00000699855.1:n.2912A>T
ENST00000699856.1:c.2460A>T ENSP00000514650.1:p.Ile820=
ENST00000699857.1:n.2468A>T
ENST00000699858.1:c.*1073A>T ENSP00000514651.1:n.*1073A>T
ENST00000699859.1:c.2331A>T ENSP00000514652.1:p.Ile777=
ENST00000699860.1:n.566A>T
ENST00000699861.1:n.2482A>T
ENST00000699862.1:n.3420A>T
ENST00000449476.7:c.2355A>T ENSP00000396018.2:p.Ile785=
ENST00000581671.2:n.2449A>T
ENST00000643543.1:c.*1167A>T ENSP00000494323.1:n.*1167A>T
ENST00000651323.1:c.2460A>T MANE Select ENSP00000498499.1:p.Ile820=
ENST00000315684.12:c.2460A>T ENSP00000313759.8:p.Ile820=
ENST00000449476.6:c.2355A>T ENSP00000396018.2:p.Ile785=
ENST00000578240.1:n.688A>T
ENST00000578537.1:c.356A>T
NM_025099.5:c.2460A>T NP_079375.3:p.Ile820=
NR_046431.1:n.2414A>T
XM_006721577.2:c.2331A>T XP_006721640.1:p.Ile777=
XM_006721578.2:c.2460A>T XP_006721641.1:p.Ile820=
XM_006721579.2:c.2460A>T XP_006721642.1:p.Ile820=
XM_011524010.1:c.2355A>T XP_011522312.1:p.Ile785=
XM_011524011.1:c.1563A>T XP_011522313.1:p.Ile521=
XR_429823.2:n.2503A>T
XR_429824.2:n.2503A>T
XR_429825.1:n.2503A>T
NM_025099.6:c.2460A>T MANE Select NP_079375.3:p.Ile820=
XM_006721577.3:c.2331A>T XP_006721640.1:p.Ile777=
XM_006721578.3:c.2460A>T XP_006721641.1:p.Ile820=
XM_011524010.2:c.2355A>T XP_011522312.1:p.Ile785=
XM_011524011.2:c.1563A>T XP_011522313.1:p.Ile521=
XR_001752639.1:n.2374A>T
XR_001752640.1:n.2503A>T
XR_001752641.1:n.2503A>T
XR_001752642.1:n.2503A>T
XR_001752643.1:n.2933A>T
XR_002958073.1:n.2503A>T
XR_429823.3:n.2503A>T
XR_429824.3:n.2503A>T
NR_046431.2:n.2375A>T