Canonical Allele Identifier: CA2246188696

Gene: CTC1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8231016_8231017delinsCT , CM000679.2:g.8231016_8231017delinsCT	GRCh38
NC_000017.10:g.8134334_8134335delinsCT , CM000679.1:g.8134334_8134335delinsCT	GRCh37
NC_000017.9:g.8075059_8075060delinsCT	NCBI36
NG_032148.1:g.22079_22080delinsAG
NG_032148.2:g.22079_22080delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000580299.2:c.2669+259_2669+260delinsAG	ENSP00000462607.2:n.2669+259_2669+260delinsAG
ENST00000581729.2:c.2669+259_2669+260delinsAG	ENSP00000462720.2:n.2669+259_2669+260delinsAG
ENST00000581967.2:n.3121+259_3121+260delinsAG
ENST00000583254.2:n.3977_3978delinsAG
ENST00000699849.1:c.1772+259_1772+260delinsAG	ENSP00000514647.1:n.1772+259_1772+260delinsAG
ENST00000699850.1:n.1932+259_1932+260delinsAG
ENST00000699851.1:n.2691+259_2691+260delinsAG
ENST00000699852.1:c.*1345+259_*1345+260delinsAG	ENSP00000514648.1:n.*1345+259_*1345+260delinsAG
ENST00000699853.1:c.2669+259_2669+260delinsAG	ENSP00000514649.1:n.2669+259_2669+260delinsAG
ENST00000699854.1:n.2462+259_2462+260delinsAG
ENST00000699855.1:n.3121+259_3121+260delinsAG
ENST00000699856.1:c.2669+259_2669+260delinsAG	ENSP00000514650.1:n.2669+259_2669+260delinsAG
ENST00000699857.1:n.2677+259_2677+260delinsAG
ENST00000699858.1:c.*1282+259_*1282+260delinsAG	ENSP00000514651.1:n.*1282+259_*1282+260delinsAG
ENST00000699859.1:c.2540+259_2540+260delinsAG	ENSP00000514652.1:n.2540+259_2540+260delinsAG
ENST00000699860.1:n.582-366_582-365delinsAG
ENST00000699861.1:n.2691+259_2691+260delinsAG
ENST00000699862.1:n.3629+259_3629+260delinsAG
ENST00000449476.7:c.2564+259_2564+260delinsAG	ENSP00000396018.2:n.2564+259_2564+260delinsAG
ENST00000581671.2:n.2658+259_2658+260delinsAG
ENST00000643543.1:c.*1376+259_*1376+260delinsAG	ENSP00000494323.1:n.*1376+259_*1376+260delinsAG
ENST00000651323.1:c.2669+259_2669+260delinsAG MANE Select	ENSP00000498499.1:n.2669+259_2669+260delinsAG
ENST00000315684.12:c.2669+259_2669+260delinsAG	ENSP00000313759.8:n.2669+259_2669+260delinsAG
ENST00000449476.6:c.2564+259_2564+260delinsAG	ENSP00000396018.2:n.2564+259_2564+260delinsAG
ENST00000578240.1:n.897+259_897+260delinsAG
ENST00000578441.5:n.170+259_170+260delinsAG
ENST00000578537.1:c.372-366_372-365delinsAG
NM_025099.5:c.2669+259_2669+260delinsAG	NP_079375.3:n.2669+259_2669+260delinsAG
NR_046431.1:n.2623+259_2623+260delinsAG
XM_006721577.2:c.2540+259_2540+260delinsAG	XP_006721640.1:n.2540+259_2540+260delinsAG
XM_006721578.2:c.2669+259_2669+260delinsAG	XP_006721641.1:n.2669+259_2669+260delinsAG
XM_006721579.2:c.2669+259_2669+260delinsAG	XP_006721642.1:n.2669+259_2669+260delinsAG
XM_011524010.1:c.2564+259_2564+260delinsAG	XP_011522312.1:n.2564+259_2564+260delinsAG
XM_011524011.1:c.1772+259_1772+260delinsAG	XP_011522313.1:n.1772+259_1772+260delinsAG
XR_429823.2:n.2712+259_2712+260delinsAG
XR_429824.2:n.2712+259_2712+260delinsAG
XR_429825.1:n.2519-366_2519-365delinsAG
NM_025099.6:c.2669+259_2669+260delinsAG MANE Select	NP_079375.3:n.2669+259_2669+260delinsAG
XM_006721577.3:c.2540+259_2540+260delinsAG	XP_006721640.1:n.2540+259_2540+260delinsAG
XM_006721578.3:c.2669+259_2669+260delinsAG	XP_006721641.1:n.2669+259_2669+260delinsAG
XM_011524010.2:c.2564+259_2564+260delinsAG	XP_011522312.1:n.2564+259_2564+260delinsAG
XM_011524011.2:c.1772+259_1772+260delinsAG	XP_011522313.1:n.1772+259_1772+260delinsAG
XR_001752639.1:n.2583+259_2583+260delinsAG
XR_001752640.1:n.2712+259_2712+260delinsAG
XR_001752641.1:n.2712+259_2712+260delinsAG
XR_001752642.1:n.2519-366_2519-365delinsAG
XR_001752643.1:n.3142+259_3142+260delinsAG
XR_002958073.1:n.2519-366_2519-365delinsAG
XR_429823.3:n.2712+259_2712+260delinsAG
XR_429824.3:n.2712+259_2712+260delinsAG
NR_046431.2:n.2584+259_2584+260delinsAG