Canonical Allele Identifier: CA2635984543

Gene: CTC1

Linked Data

• gnomAD v4: 17-8231140-C-CAAA

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8231147_8231149dup , CM000679.2:g.8231147_8231149dup	GRCh38
NC_000017.10:g.8134465_8134467dup , CM000679.1:g.8134465_8134467dup	GRCh37
NC_000017.9:g.8075190_8075192dup	NCBI36
NG_032148.1:g.21953_21955dup
NG_032148.2:g.21953_21955dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000580299.2:c.2669+133_2669+135dup	ENSP00000462607.2:n.2669+133_2669+135dup
ENST00000581729.2:c.2669+133_2669+135dup	ENSP00000462720.2:n.2669+133_2669+135dup
ENST00000581967.2:n.3121+133_3121+135dup
ENST00000583254.2:n.3851_3853dup
ENST00000699849.1:c.1772+133_1772+135dup	ENSP00000514647.1:n.1772+133_1772+135dup
ENST00000699850.1:n.1932+133_1932+135dup
ENST00000699851.1:n.2691+133_2691+135dup
ENST00000699852.1:c.*1345+133_*1345+135dup	ENSP00000514648.1:n.*1345+133_*1345+135dup
ENST00000699853.1:c.2669+133_2669+135dup	ENSP00000514649.1:n.2669+133_2669+135dup
ENST00000699854.1:n.2462+133_2462+135dup
ENST00000699855.1:n.3121+133_3121+135dup
ENST00000699856.1:c.2669+133_2669+135dup	ENSP00000514650.1:n.2669+133_2669+135dup
ENST00000699857.1:n.2677+133_2677+135dup
ENST00000699858.1:c.*1282+133_*1282+135dup	ENSP00000514651.1:n.*1282+133_*1282+135dup
ENST00000699859.1:c.2540+133_2540+135dup	ENSP00000514652.1:n.2540+133_2540+135dup
ENST00000699860.1:n.582-492_582-490dup
ENST00000699861.1:n.2691+133_2691+135dup
ENST00000699862.1:n.3629+133_3629+135dup
ENST00000449476.7:c.2564+133_2564+135dup	ENSP00000396018.2:n.2564+133_2564+135dup
ENST00000581671.2:n.2658+133_2658+135dup
ENST00000643543.1:c.*1376+133_*1376+135dup	ENSP00000494323.1:n.*1376+133_*1376+135dup
ENST00000651323.1:c.2669+133_2669+135dup MANE Select	ENSP00000498499.1:n.2669+133_2669+135dup
ENST00000315684.12:c.2669+133_2669+135dup	ENSP00000313759.8:n.2669+133_2669+135dup
ENST00000449476.6:c.2564+133_2564+135dup	ENSP00000396018.2:n.2564+133_2564+135dup
ENST00000578240.1:n.897+133_897+135dup
ENST00000578441.5:n.170+133_170+135dup
ENST00000578537.1:c.372-492_372-490dup
NM_025099.5:c.2669+133_2669+135dup	NP_079375.3:n.2669+133_2669+135dup
NR_046431.1:n.2623+133_2623+135dup
XM_006721577.2:c.2540+133_2540+135dup	XP_006721640.1:n.2540+133_2540+135dup
XM_006721578.2:c.2669+133_2669+135dup	XP_006721641.1:n.2669+133_2669+135dup
XM_006721579.2:c.2669+133_2669+135dup	XP_006721642.1:n.2669+133_2669+135dup
XM_011524010.1:c.2564+133_2564+135dup	XP_011522312.1:n.2564+133_2564+135dup
XM_011524011.1:c.1772+133_1772+135dup	XP_011522313.1:n.1772+133_1772+135dup
XR_429823.2:n.2712+133_2712+135dup
XR_429824.2:n.2712+133_2712+135dup
XR_429825.1:n.2519-492_2519-490dup
NM_025099.6:c.2669+133_2669+135dup MANE Select	NP_079375.3:n.2669+133_2669+135dup
XM_006721577.3:c.2540+133_2540+135dup	XP_006721640.1:n.2540+133_2540+135dup
XM_006721578.3:c.2669+133_2669+135dup	XP_006721641.1:n.2669+133_2669+135dup
XM_011524010.2:c.2564+133_2564+135dup	XP_011522312.1:n.2564+133_2564+135dup
XM_011524011.2:c.1772+133_1772+135dup	XP_011522313.1:n.1772+133_1772+135dup
XR_001752639.1:n.2583+133_2583+135dup
XR_001752640.1:n.2712+133_2712+135dup
XR_001752641.1:n.2712+133_2712+135dup
XR_001752642.1:n.2519-492_2519-490dup
XR_001752643.1:n.3142+133_3142+135dup
XR_002958073.1:n.2519-492_2519-490dup
XR_429823.3:n.2712+133_2712+135dup
XR_429824.3:n.2712+133_2712+135dup
NR_046431.2:n.2584+133_2584+135dup