Canonical Allele Identifier: CA2635984330

Gene: CTC1

Linked Data

• gnomAD v4: 17-8230950-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8230950A>T , CM000679.2:g.8230950A>T	GRCh38
NC_000017.10:g.8134268A>T , CM000679.1:g.8134268A>T	GRCh37
NC_000017.9:g.8074993A>T	NCBI36
NG_032148.1:g.22146T>A
NG_032148.2:g.22146T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000580299.2:c.2670-299T>A	ENSP00000462607.2:n.2670-299T>A
ENST00000581729.2:c.2670-299T>A	ENSP00000462720.2:n.2670-299T>A
ENST00000581967.2:n.3122-299T>A
ENST00000583254.2:n.4044T>A
ENST00000699849.1:c.1773-299T>A	ENSP00000514647.1:n.1773-299T>A
ENST00000699850.1:n.1933-299T>A
ENST00000699851.1:n.2692-299T>A
ENST00000699852.1:c.*1346-299T>A	ENSP00000514648.1:n.*1346-299T>A
ENST00000699853.1:c.2670-299T>A	ENSP00000514649.1:n.2670-299T>A
ENST00000699854.1:n.2463-299T>A
ENST00000699855.1:n.3122-299T>A
ENST00000699856.1:c.2670-299T>A	ENSP00000514650.1:n.2670-299T>A
ENST00000699857.1:n.2678-299T>A
ENST00000699858.1:c.*1283-299T>A	ENSP00000514651.1:n.*1283-299T>A
ENST00000699859.1:c.2541-299T>A	ENSP00000514652.1:n.2541-299T>A
ENST00000699860.1:n.582-299T>A
ENST00000699861.1:n.2692-299T>A
ENST00000699862.1:n.3630-299T>A
ENST00000449476.7:c.2565-299T>A	ENSP00000396018.2:n.2565-299T>A
ENST00000581671.2:n.2659-299T>A
ENST00000643543.1:c.*1377-299T>A	ENSP00000494323.1:n.*1377-299T>A
ENST00000651323.1:c.2670-299T>A MANE Select	ENSP00000498499.1:n.2670-299T>A
ENST00000315684.12:c.2670-299T>A	ENSP00000313759.8:n.2670-299T>A
ENST00000449476.6:c.2565-299T>A	ENSP00000396018.2:n.2565-299T>A
ENST00000578240.1:n.898-299T>A
ENST00000578441.5:n.171-299T>A
ENST00000578537.1:c.372-299T>A
NM_025099.5:c.2670-299T>A	NP_079375.3:n.2670-299T>A
NR_046431.1:n.2624-299T>A
XM_006721577.2:c.2541-299T>A	XP_006721640.1:n.2541-299T>A
XM_006721578.2:c.2670-299T>A	XP_006721641.1:n.2670-299T>A
XM_006721579.2:c.2670-299T>A	XP_006721642.1:n.2670-299T>A
XM_011524010.1:c.2565-299T>A	XP_011522312.1:n.2565-299T>A
XM_011524011.1:c.1773-299T>A	XP_011522313.1:n.1773-299T>A
XR_429823.2:n.2713-299T>A
XR_429824.2:n.2713-299T>A
XR_429825.1:n.2519-299T>A
NM_025099.6:c.2670-299T>A MANE Select	NP_079375.3:n.2670-299T>A
XM_006721577.3:c.2541-299T>A	XP_006721640.1:n.2541-299T>A
XM_006721578.3:c.2670-299T>A	XP_006721641.1:n.2670-299T>A
XM_011524010.2:c.2565-299T>A	XP_011522312.1:n.2565-299T>A
XM_011524011.2:c.1773-299T>A	XP_011522313.1:n.1773-299T>A
XR_001752639.1:n.2584-299T>A
XR_001752640.1:n.2713-299T>A
XR_001752641.1:n.2713-299T>A
XR_001752642.1:n.2519-299T>A
XR_001752643.1:n.3143-299T>A
XR_002958073.1:n.2519-299T>A
XR_429823.3:n.2713-299T>A
XR_429824.3:n.2713-299T>A
NR_046431.2:n.2585-299T>A