Canonical Allele Identifier: CA2246188778

Gene: CTC1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8231154_8231155delinsCA , CM000679.2:g.8231154_8231155delinsCA	GRCh38
NC_000017.10:g.8134472_8134473delinsCA , CM000679.1:g.8134472_8134473delinsCA	GRCh37
NC_000017.9:g.8075197_8075198delinsCA	NCBI36
NG_032148.1:g.21941_21942delinsTG
NG_032148.2:g.21941_21942delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000580299.2:c.2669+121_2669+122delinsTG	ENSP00000462607.2:n.2669+121_2669+122delinsTG
ENST00000581729.2:c.2669+121_2669+122delinsTG	ENSP00000462720.2:n.2669+121_2669+122delinsTG
ENST00000581967.2:n.3121+121_3121+122delinsTG
ENST00000583254.2:n.3839_3840delinsTG
ENST00000699849.1:c.1772+121_1772+122delinsTG	ENSP00000514647.1:n.1772+121_1772+122delinsTG
ENST00000699850.1:n.1932+121_1932+122delinsTG
ENST00000699851.1:n.2691+121_2691+122delinsTG
ENST00000699852.1:c.*1345+121_*1345+122delinsTG	ENSP00000514648.1:n.*1345+121_*1345+122delinsTG
ENST00000699853.1:c.2669+121_2669+122delinsTG	ENSP00000514649.1:n.2669+121_2669+122delinsTG
ENST00000699854.1:n.2462+121_2462+122delinsTG
ENST00000699855.1:n.3121+121_3121+122delinsTG
ENST00000699856.1:c.2669+121_2669+122delinsTG	ENSP00000514650.1:n.2669+121_2669+122delinsTG
ENST00000699857.1:n.2677+121_2677+122delinsTG
ENST00000699858.1:c.*1282+121_*1282+122delinsTG	ENSP00000514651.1:n.*1282+121_*1282+122delinsTG
ENST00000699859.1:c.2540+121_2540+122delinsTG	ENSP00000514652.1:n.2540+121_2540+122delinsTG
ENST00000699860.1:n.582-504_582-503delinsTG
ENST00000699861.1:n.2691+121_2691+122delinsTG
ENST00000699862.1:n.3629+121_3629+122delinsTG
ENST00000449476.7:c.2564+121_2564+122delinsTG	ENSP00000396018.2:n.2564+121_2564+122delinsTG
ENST00000581671.2:n.2658+121_2658+122delinsTG
ENST00000643543.1:c.*1376+121_*1376+122delinsTG	ENSP00000494323.1:n.*1376+121_*1376+122delinsTG
ENST00000651323.1:c.2669+121_2669+122delinsTG MANE Select	ENSP00000498499.1:n.2669+121_2669+122delinsTG
ENST00000315684.12:c.2669+121_2669+122delinsTG	ENSP00000313759.8:n.2669+121_2669+122delinsTG
ENST00000449476.6:c.2564+121_2564+122delinsTG	ENSP00000396018.2:n.2564+121_2564+122delinsTG
ENST00000578240.1:n.897+121_897+122delinsTG
ENST00000578441.5:n.170+121_170+122delinsTG
ENST00000578537.1:c.372-504_372-503delinsTG
NM_025099.5:c.2669+121_2669+122delinsTG	NP_079375.3:n.2669+121_2669+122delinsTG
NR_046431.1:n.2623+121_2623+122delinsTG
XM_006721577.2:c.2540+121_2540+122delinsTG	XP_006721640.1:n.2540+121_2540+122delinsTG
XM_006721578.2:c.2669+121_2669+122delinsTG	XP_006721641.1:n.2669+121_2669+122delinsTG
XM_006721579.2:c.2669+121_2669+122delinsTG	XP_006721642.1:n.2669+121_2669+122delinsTG
XM_011524010.1:c.2564+121_2564+122delinsTG	XP_011522312.1:n.2564+121_2564+122delinsTG
XM_011524011.1:c.1772+121_1772+122delinsTG	XP_011522313.1:n.1772+121_1772+122delinsTG
XR_429823.2:n.2712+121_2712+122delinsTG
XR_429824.2:n.2712+121_2712+122delinsTG
XR_429825.1:n.2519-504_2519-503delinsTG
NM_025099.6:c.2669+121_2669+122delinsTG MANE Select	NP_079375.3:n.2669+121_2669+122delinsTG
XM_006721577.3:c.2540+121_2540+122delinsTG	XP_006721640.1:n.2540+121_2540+122delinsTG
XM_006721578.3:c.2669+121_2669+122delinsTG	XP_006721641.1:n.2669+121_2669+122delinsTG
XM_011524010.2:c.2564+121_2564+122delinsTG	XP_011522312.1:n.2564+121_2564+122delinsTG
XM_011524011.2:c.1772+121_1772+122delinsTG	XP_011522313.1:n.1772+121_1772+122delinsTG
XR_001752639.1:n.2583+121_2583+122delinsTG
XR_001752640.1:n.2712+121_2712+122delinsTG
XR_001752641.1:n.2712+121_2712+122delinsTG
XR_001752642.1:n.2519-504_2519-503delinsTG
XR_001752643.1:n.3142+121_3142+122delinsTG
XR_002958073.1:n.2519-504_2519-503delinsTG
XR_429823.3:n.2712+121_2712+122delinsTG
XR_429824.3:n.2712+121_2712+122delinsTG
NR_046431.2:n.2584+121_2584+122delinsTG