Canonical Allele Identifier: CA2635984549

Gene: CTC1

Linked Data

• gnomAD v4: 17-8231143-A-AAAC

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8231145_8231146insCAA , CM000679.2:g.8231145_8231146insCAA	GRCh38
NC_000017.10:g.8134463_8134464insCAA , CM000679.1:g.8134463_8134464insCAA	GRCh37
NC_000017.9:g.8075188_8075189insCAA	NCBI36
NG_032148.1:g.21952_21953insGTT
NG_032148.2:g.21952_21953insGTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000580299.2:c.2669+132_2669+133insGTT	ENSP00000462607.2:n.2669+132_2669+133insGTT
ENST00000581729.2:c.2669+132_2669+133insGTT	ENSP00000462720.2:n.2669+132_2669+133insGTT
ENST00000581967.2:n.3121+132_3121+133insGTT
ENST00000583254.2:n.3850_3851insGTT
ENST00000699849.1:c.1772+132_1772+133insGTT	ENSP00000514647.1:n.1772+132_1772+133insGTT
ENST00000699850.1:n.1932+132_1932+133insGTT
ENST00000699851.1:n.2691+132_2691+133insGTT
ENST00000699852.1:c.*1345+132_*1345+133insGTT	ENSP00000514648.1:n.*1345+132_*1345+133insGTT
ENST00000699853.1:c.2669+132_2669+133insGTT	ENSP00000514649.1:n.2669+132_2669+133insGTT
ENST00000699854.1:n.2462+132_2462+133insGTT
ENST00000699855.1:n.3121+132_3121+133insGTT
ENST00000699856.1:c.2669+132_2669+133insGTT	ENSP00000514650.1:n.2669+132_2669+133insGTT
ENST00000699857.1:n.2677+132_2677+133insGTT
ENST00000699858.1:c.*1282+132_*1282+133insGTT	ENSP00000514651.1:n.*1282+132_*1282+133insGTT
ENST00000699859.1:c.2540+132_2540+133insGTT	ENSP00000514652.1:n.2540+132_2540+133insGTT
ENST00000699860.1:n.582-493_582-492insGTT
ENST00000699861.1:n.2691+132_2691+133insGTT
ENST00000699862.1:n.3629+132_3629+133insGTT
ENST00000449476.7:c.2564+132_2564+133insGTT	ENSP00000396018.2:n.2564+132_2564+133insGTT
ENST00000581671.2:n.2658+132_2658+133insGTT
ENST00000643543.1:c.*1376+132_*1376+133insGTT	ENSP00000494323.1:n.*1376+132_*1376+133insGTT
ENST00000651323.1:c.2669+132_2669+133insGTT MANE Select	ENSP00000498499.1:n.2669+132_2669+133insGTT
ENST00000315684.12:c.2669+132_2669+133insGTT	ENSP00000313759.8:n.2669+132_2669+133insGTT
ENST00000449476.6:c.2564+132_2564+133insGTT	ENSP00000396018.2:n.2564+132_2564+133insGTT
ENST00000578240.1:n.897+132_897+133insGTT
ENST00000578441.5:n.170+132_170+133insGTT
ENST00000578537.1:c.372-493_372-492insGTT
NM_025099.5:c.2669+132_2669+133insGTT	NP_079375.3:n.2669+132_2669+133insGTT
NR_046431.1:n.2623+132_2623+133insGTT
XM_006721577.2:c.2540+132_2540+133insGTT	XP_006721640.1:n.2540+132_2540+133insGTT
XM_006721578.2:c.2669+132_2669+133insGTT	XP_006721641.1:n.2669+132_2669+133insGTT
XM_006721579.2:c.2669+132_2669+133insGTT	XP_006721642.1:n.2669+132_2669+133insGTT
XM_011524010.1:c.2564+132_2564+133insGTT	XP_011522312.1:n.2564+132_2564+133insGTT
XM_011524011.1:c.1772+132_1772+133insGTT	XP_011522313.1:n.1772+132_1772+133insGTT
XR_429823.2:n.2712+132_2712+133insGTT
XR_429824.2:n.2712+132_2712+133insGTT
XR_429825.1:n.2519-493_2519-492insGTT
NM_025099.6:c.2669+132_2669+133insGTT MANE Select	NP_079375.3:n.2669+132_2669+133insGTT
XM_006721577.3:c.2540+132_2540+133insGTT	XP_006721640.1:n.2540+132_2540+133insGTT
XM_006721578.3:c.2669+132_2669+133insGTT	XP_006721641.1:n.2669+132_2669+133insGTT
XM_011524010.2:c.2564+132_2564+133insGTT	XP_011522312.1:n.2564+132_2564+133insGTT
XM_011524011.2:c.1772+132_1772+133insGTT	XP_011522313.1:n.1772+132_1772+133insGTT
XR_001752639.1:n.2583+132_2583+133insGTT
XR_001752640.1:n.2712+132_2712+133insGTT
XR_001752641.1:n.2712+132_2712+133insGTT
XR_001752642.1:n.2519-493_2519-492insGTT
XR_001752643.1:n.3142+132_3142+133insGTT
XR_002958073.1:n.2519-493_2519-492insGTT
XR_429823.3:n.2712+132_2712+133insGTT
XR_429824.3:n.2712+132_2712+133insGTT
NR_046431.2:n.2584+132_2584+133insGTT