Canonical Allele Identifier: CA2635984540

Gene: CTC1

Linked Data

• gnomAD v4: 17-8231140-CAAAA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8231146_8231149del , CM000679.2:g.8231146_8231149del	GRCh38
NC_000017.10:g.8134464_8134467del , CM000679.1:g.8134464_8134467del	GRCh37
NC_000017.9:g.8075189_8075192del	NCBI36
NG_032148.1:g.21952_21955del
NG_032148.2:g.21952_21955del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000580299.2:c.2669+132_2669+135del	ENSP00000462607.2:n.2669+132_2669+135del
ENST00000581729.2:c.2669+132_2669+135del	ENSP00000462720.2:n.2669+132_2669+135del
ENST00000581967.2:n.3121+132_3121+135del
ENST00000583254.2:n.3850_3853del
ENST00000699849.1:c.1772+132_1772+135del	ENSP00000514647.1:n.1772+132_1772+135del
ENST00000699850.1:n.1932+132_1932+135del
ENST00000699851.1:n.2691+132_2691+135del
ENST00000699852.1:c.*1345+132_*1345+135del	ENSP00000514648.1:n.*1345+132_*1345+135del
ENST00000699853.1:c.2669+132_2669+135del	ENSP00000514649.1:n.2669+132_2669+135del
ENST00000699854.1:n.2462+132_2462+135del
ENST00000699855.1:n.3121+132_3121+135del
ENST00000699856.1:c.2669+132_2669+135del	ENSP00000514650.1:n.2669+132_2669+135del
ENST00000699857.1:n.2677+132_2677+135del
ENST00000699858.1:c.*1282+132_*1282+135del	ENSP00000514651.1:n.*1282+132_*1282+135del
ENST00000699859.1:c.2540+132_2540+135del	ENSP00000514652.1:n.2540+132_2540+135del
ENST00000699860.1:n.582-493_582-490del
ENST00000699861.1:n.2691+132_2691+135del
ENST00000699862.1:n.3629+132_3629+135del
ENST00000449476.7:c.2564+132_2564+135del	ENSP00000396018.2:n.2564+132_2564+135del
ENST00000581671.2:n.2658+132_2658+135del
ENST00000643543.1:c.*1376+132_*1376+135del	ENSP00000494323.1:n.*1376+132_*1376+135del
ENST00000651323.1:c.2669+132_2669+135del MANE Select	ENSP00000498499.1:n.2669+132_2669+135del
ENST00000315684.12:c.2669+132_2669+135del	ENSP00000313759.8:n.2669+132_2669+135del
ENST00000449476.6:c.2564+132_2564+135del	ENSP00000396018.2:n.2564+132_2564+135del
ENST00000578240.1:n.897+132_897+135del
ENST00000578441.5:n.170+132_170+135del
ENST00000578537.1:c.372-493_372-490del
NM_025099.5:c.2669+132_2669+135del	NP_079375.3:n.2669+132_2669+135del
NR_046431.1:n.2623+132_2623+135del
XM_006721577.2:c.2540+132_2540+135del	XP_006721640.1:n.2540+132_2540+135del
XM_006721578.2:c.2669+132_2669+135del	XP_006721641.1:n.2669+132_2669+135del
XM_006721579.2:c.2669+132_2669+135del	XP_006721642.1:n.2669+132_2669+135del
XM_011524010.1:c.2564+132_2564+135del	XP_011522312.1:n.2564+132_2564+135del
XM_011524011.1:c.1772+132_1772+135del	XP_011522313.1:n.1772+132_1772+135del
XR_429823.2:n.2712+132_2712+135del
XR_429824.2:n.2712+132_2712+135del
XR_429825.1:n.2519-493_2519-490del
NM_025099.6:c.2669+132_2669+135del MANE Select	NP_079375.3:n.2669+132_2669+135del
XM_006721577.3:c.2540+132_2540+135del	XP_006721640.1:n.2540+132_2540+135del
XM_006721578.3:c.2669+132_2669+135del	XP_006721641.1:n.2669+132_2669+135del
XM_011524010.2:c.2564+132_2564+135del	XP_011522312.1:n.2564+132_2564+135del
XM_011524011.2:c.1772+132_1772+135del	XP_011522313.1:n.1772+132_1772+135del
XR_001752639.1:n.2583+132_2583+135del
XR_001752640.1:n.2712+132_2712+135del
XR_001752641.1:n.2712+132_2712+135del
XR_001752642.1:n.2519-493_2519-490del
XR_001752643.1:n.3142+132_3142+135del
XR_002958073.1:n.2519-493_2519-490del
XR_429823.3:n.2712+132_2712+135del
XR_429824.3:n.2712+132_2712+135del
NR_046431.2:n.2584+132_2584+135del