Canonical Allele Identifier: CA2635984286

Gene: CTC1

Linked Data

• gnomAD v4: 17-8230933-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8230933T>C , CM000679.2:g.8230933T>C	GRCh38
NC_000017.10:g.8134251T>C , CM000679.1:g.8134251T>C	GRCh37
NC_000017.9:g.8074976T>C	NCBI36
NG_032148.1:g.22163A>G
NG_032148.2:g.22163A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000580299.2:c.2670-282A>G	ENSP00000462607.2:n.2670-282A>G
ENST00000581729.2:c.2670-282A>G	ENSP00000462720.2:n.2670-282A>G
ENST00000581967.2:n.3122-282A>G
ENST00000583254.2:n.4061A>G
ENST00000699849.1:c.1773-282A>G	ENSP00000514647.1:n.1773-282A>G
ENST00000699850.1:n.1933-282A>G
ENST00000699851.1:n.2692-282A>G
ENST00000699852.1:c.*1346-282A>G	ENSP00000514648.1:n.*1346-282A>G
ENST00000699853.1:c.2670-282A>G	ENSP00000514649.1:n.2670-282A>G
ENST00000699854.1:n.2463-282A>G
ENST00000699855.1:n.3122-282A>G
ENST00000699856.1:c.2670-282A>G	ENSP00000514650.1:n.2670-282A>G
ENST00000699857.1:n.2678-282A>G
ENST00000699858.1:c.*1283-282A>G	ENSP00000514651.1:n.*1283-282A>G
ENST00000699859.1:c.2541-282A>G	ENSP00000514652.1:n.2541-282A>G
ENST00000699860.1:n.582-282A>G
ENST00000699861.1:n.2692-282A>G
ENST00000699862.1:n.3630-282A>G
ENST00000449476.7:c.2565-282A>G	ENSP00000396018.2:n.2565-282A>G
ENST00000581671.2:n.2659-282A>G
ENST00000643543.1:c.*1377-282A>G	ENSP00000494323.1:n.*1377-282A>G
ENST00000651323.1:c.2670-282A>G MANE Select	ENSP00000498499.1:n.2670-282A>G
ENST00000315684.12:c.2670-282A>G	ENSP00000313759.8:n.2670-282A>G
ENST00000449476.6:c.2565-282A>G	ENSP00000396018.2:n.2565-282A>G
ENST00000578240.1:n.898-282A>G
ENST00000578441.5:n.171-282A>G
ENST00000578537.1:c.372-282A>G
ENST00000584439.1:n.1A>G
NM_025099.5:c.2670-282A>G	NP_079375.3:n.2670-282A>G
NR_046431.1:n.2624-282A>G
XM_006721577.2:c.2541-282A>G	XP_006721640.1:n.2541-282A>G
XM_006721578.2:c.2670-282A>G	XP_006721641.1:n.2670-282A>G
XM_006721579.2:c.2670-282A>G	XP_006721642.1:n.2670-282A>G
XM_011524010.1:c.2565-282A>G	XP_011522312.1:n.2565-282A>G
XM_011524011.1:c.1773-282A>G	XP_011522313.1:n.1773-282A>G
XR_429823.2:n.2713-282A>G
XR_429824.2:n.2713-282A>G
XR_429825.1:n.2519-282A>G
NM_025099.6:c.2670-282A>G MANE Select	NP_079375.3:n.2670-282A>G
XM_006721577.3:c.2541-282A>G	XP_006721640.1:n.2541-282A>G
XM_006721578.3:c.2670-282A>G	XP_006721641.1:n.2670-282A>G
XM_011524010.2:c.2565-282A>G	XP_011522312.1:n.2565-282A>G
XM_011524011.2:c.1773-282A>G	XP_011522313.1:n.1773-282A>G
XR_001752639.1:n.2584-282A>G
XR_001752640.1:n.2713-282A>G
XR_001752641.1:n.2713-282A>G
XR_001752642.1:n.2519-282A>G
XR_001752643.1:n.3143-282A>G
XR_002958073.1:n.2519-282A>G
XR_429823.3:n.2713-282A>G
XR_429824.3:n.2713-282A>G
NR_046431.2:n.2585-282A>G