Canonical Allele Identifier: CA2635984532

Gene: CTC1

Linked Data

• gnomAD v4: 17-8231139-T-TA

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8231139_8231140insA , CM000679.2:g.8231139_8231140insA	GRCh38
NC_000017.10:g.8134457_8134458insA , CM000679.1:g.8134457_8134458insA	GRCh37
NC_000017.9:g.8075182_8075183insA	NCBI36
NG_032148.1:g.21956_21957insT
NG_032148.2:g.21956_21957insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000580299.2:c.2669+136_2669+137insT	ENSP00000462607.2:n.2669+136_2669+137insT
ENST00000581729.2:c.2669+136_2669+137insT	ENSP00000462720.2:n.2669+136_2669+137insT
ENST00000581967.2:n.3121+136_3121+137insT
ENST00000583254.2:n.3854_3855insT
ENST00000699849.1:c.1772+136_1772+137insT	ENSP00000514647.1:n.1772+136_1772+137insT
ENST00000699850.1:n.1932+136_1932+137insT
ENST00000699851.1:n.2691+136_2691+137insT
ENST00000699852.1:c.*1345+136_*1345+137insT	ENSP00000514648.1:n.*1345+136_*1345+137insT
ENST00000699853.1:c.2669+136_2669+137insT	ENSP00000514649.1:n.2669+136_2669+137insT
ENST00000699854.1:n.2462+136_2462+137insT
ENST00000699855.1:n.3121+136_3121+137insT
ENST00000699856.1:c.2669+136_2669+137insT	ENSP00000514650.1:n.2669+136_2669+137insT
ENST00000699857.1:n.2677+136_2677+137insT
ENST00000699858.1:c.*1282+136_*1282+137insT	ENSP00000514651.1:n.*1282+136_*1282+137insT
ENST00000699859.1:c.2540+136_2540+137insT	ENSP00000514652.1:n.2540+136_2540+137insT
ENST00000699860.1:n.582-489_582-488insT
ENST00000699861.1:n.2691+136_2691+137insT
ENST00000699862.1:n.3629+136_3629+137insT
ENST00000449476.7:c.2564+136_2564+137insT	ENSP00000396018.2:n.2564+136_2564+137insT
ENST00000581671.2:n.2658+136_2658+137insT
ENST00000643543.1:c.*1376+136_*1376+137insT	ENSP00000494323.1:n.*1376+136_*1376+137insT
ENST00000651323.1:c.2669+136_2669+137insT MANE Select	ENSP00000498499.1:n.2669+136_2669+137insT
ENST00000315684.12:c.2669+136_2669+137insT	ENSP00000313759.8:n.2669+136_2669+137insT
ENST00000449476.6:c.2564+136_2564+137insT	ENSP00000396018.2:n.2564+136_2564+137insT
ENST00000578240.1:n.897+136_897+137insT
ENST00000578441.5:n.170+136_170+137insT
ENST00000578537.1:c.372-489_372-488insT
NM_025099.5:c.2669+136_2669+137insT	NP_079375.3:n.2669+136_2669+137insT
NR_046431.1:n.2623+136_2623+137insT
XM_006721577.2:c.2540+136_2540+137insT	XP_006721640.1:n.2540+136_2540+137insT
XM_006721578.2:c.2669+136_2669+137insT	XP_006721641.1:n.2669+136_2669+137insT
XM_006721579.2:c.2669+136_2669+137insT	XP_006721642.1:n.2669+136_2669+137insT
XM_011524010.1:c.2564+136_2564+137insT	XP_011522312.1:n.2564+136_2564+137insT
XM_011524011.1:c.1772+136_1772+137insT	XP_011522313.1:n.1772+136_1772+137insT
XR_429823.2:n.2712+136_2712+137insT
XR_429824.2:n.2712+136_2712+137insT
XR_429825.1:n.2519-489_2519-488insT
NM_025099.6:c.2669+136_2669+137insT MANE Select	NP_079375.3:n.2669+136_2669+137insT
XM_006721577.3:c.2540+136_2540+137insT	XP_006721640.1:n.2540+136_2540+137insT
XM_006721578.3:c.2669+136_2669+137insT	XP_006721641.1:n.2669+136_2669+137insT
XM_011524010.2:c.2564+136_2564+137insT	XP_011522312.1:n.2564+136_2564+137insT
XM_011524011.2:c.1772+136_1772+137insT	XP_011522313.1:n.1772+136_1772+137insT
XR_001752639.1:n.2583+136_2583+137insT
XR_001752640.1:n.2712+136_2712+137insT
XR_001752641.1:n.2712+136_2712+137insT
XR_001752642.1:n.2519-489_2519-488insT
XR_001752643.1:n.3142+136_3142+137insT
XR_002958073.1:n.2519-489_2519-488insT
XR_429823.3:n.2712+136_2712+137insT
XR_429824.3:n.2712+136_2712+137insT
NR_046431.2:n.2584+136_2584+137insT