Canonical Allele Identifier: CA397976569

Gene: CTC1

Linked Data

• ClinVar Variation Id: 2084951
• ClinVar RCV Id: RCV002996031
• MyVariant Identifiers: chr17:g.8135060A>G (hg19) ; chr17:g.8231742A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8231742A>G , CM000679.2:g.8231742A>G	GRCh38
NC_000017.10:g.8135060A>G , CM000679.1:g.8135060A>G	GRCh37
NC_000017.9:g.8075785A>G	NCBI36
NG_032148.1:g.21354T>C
NG_032148.2:g.21354T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000580299.2:c.2459T>C	ENSP00000462607.2:p.Ile820Thr
ENST00000581729.2:c.2459T>C	ENSP00000462720.2:p.Ile820Thr
ENST00000581967.2:n.2911T>C
ENST00000583254.2:n.3252T>C
ENST00000699849.1:c.1562T>C	ENSP00000514647.1:p.Ile521Thr
ENST00000699850.1:n.1722T>C
ENST00000699851.1:n.2481T>C
ENST00000699852.1:c.*1135T>C	ENSP00000514648.1:n.*1135T>C
ENST00000699853.1:c.2459T>C	ENSP00000514649.1:p.Ile820Thr
ENST00000699854.1:n.2252T>C
ENST00000699855.1:n.2911T>C
ENST00000699856.1:c.2459T>C	ENSP00000514650.1:p.Ile820Thr
ENST00000699857.1:n.2467T>C
ENST00000699858.1:c.*1072T>C	ENSP00000514651.1:n.*1072T>C
ENST00000699859.1:c.2330T>C	ENSP00000514652.1:p.Ile777Thr
ENST00000699860.1:n.565T>C
ENST00000699861.1:n.2481T>C
ENST00000699862.1:n.3419T>C
ENST00000449476.7:c.2354T>C	ENSP00000396018.2:p.Ile785Thr
ENST00000581671.2:n.2448T>C
ENST00000643543.1:c.*1166T>C	ENSP00000494323.1:n.*1166T>C
ENST00000651323.1:c.2459T>C MANE Select	ENSP00000498499.1:p.Ile820Thr
ENST00000315684.12:c.2459T>C	ENSP00000313759.8:p.Ile820Thr
ENST00000449476.6:c.2354T>C	ENSP00000396018.2:p.Ile785Thr
ENST00000578240.1:n.687T>C
ENST00000578537.1:c.355T>C
NM_025099.5:c.2459T>C	NP_079375.3:p.Ile820Thr
NR_046431.1:n.2413T>C
XM_006721577.2:c.2330T>C	XP_006721640.1:p.Ile777Thr
XM_006721578.2:c.2459T>C	XP_006721641.1:p.Ile820Thr
XM_006721579.2:c.2459T>C	XP_006721642.1:p.Ile820Thr
XM_011524010.1:c.2354T>C	XP_011522312.1:p.Ile785Thr
XM_011524011.1:c.1562T>C	XP_011522313.1:p.Ile521Thr
XR_429823.2:n.2502T>C
XR_429824.2:n.2502T>C
XR_429825.1:n.2502T>C
NM_025099.6:c.2459T>C MANE Select	NP_079375.3:p.Ile820Thr
XM_006721577.3:c.2330T>C	XP_006721640.1:p.Ile777Thr
XM_006721578.3:c.2459T>C	XP_006721641.1:p.Ile820Thr
XM_011524010.2:c.2354T>C	XP_011522312.1:p.Ile785Thr
XM_011524011.2:c.1562T>C	XP_011522313.1:p.Ile521Thr
XR_001752639.1:n.2373T>C
XR_001752640.1:n.2502T>C
XR_001752641.1:n.2502T>C
XR_001752642.1:n.2502T>C
XR_001752643.1:n.2932T>C
XR_002958073.1:n.2502T>C
XR_429823.3:n.2502T>C
XR_429824.3:n.2502T>C
NR_046431.2:n.2374T>C