Canonical Allele Identifier: CA2635984676

Gene: CTC1

Linked Data

• gnomAD v4: 17-8231237-A-AGT

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8231239_8231240dup , CM000679.2:g.8231239_8231240dup	GRCh38
NC_000017.10:g.8134557_8134558dup , CM000679.1:g.8134557_8134558dup	GRCh37
NC_000017.9:g.8075282_8075283dup	NCBI36
NG_032148.1:g.21857_21858dup
NG_032148.2:g.21857_21858dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000580299.2:c.2669+37_2669+38dup	ENSP00000462607.2:n.2669+37_2669+38dup
ENST00000581729.2:c.2669+37_2669+38dup	ENSP00000462720.2:n.2669+37_2669+38dup
ENST00000581967.2:n.3121+37_3121+38dup
ENST00000583254.2:n.3755_3756dup
ENST00000699849.1:c.1772+37_1772+38dup	ENSP00000514647.1:n.1772+37_1772+38dup
ENST00000699850.1:n.1932+37_1932+38dup
ENST00000699851.1:n.2691+37_2691+38dup
ENST00000699852.1:c.*1345+37_*1345+38dup	ENSP00000514648.1:n.*1345+37_*1345+38dup
ENST00000699853.1:c.2669+37_2669+38dup	ENSP00000514649.1:n.2669+37_2669+38dup
ENST00000699854.1:n.2462+37_2462+38dup
ENST00000699855.1:n.3121+37_3121+38dup
ENST00000699856.1:c.2669+37_2669+38dup	ENSP00000514650.1:n.2669+37_2669+38dup
ENST00000699857.1:n.2677+37_2677+38dup
ENST00000699858.1:c.*1282+37_*1282+38dup	ENSP00000514651.1:n.*1282+37_*1282+38dup
ENST00000699859.1:c.2540+37_2540+38dup	ENSP00000514652.1:n.2540+37_2540+38dup
ENST00000699860.1:n.581+487_581+488dup
ENST00000699861.1:n.2691+37_2691+38dup
ENST00000699862.1:n.3629+37_3629+38dup
ENST00000449476.7:c.2564+37_2564+38dup	ENSP00000396018.2:n.2564+37_2564+38dup
ENST00000581671.2:n.2658+37_2658+38dup
ENST00000643543.1:c.*1376+37_*1376+38dup	ENSP00000494323.1:n.*1376+37_*1376+38dup
ENST00000651323.1:c.2669+37_2669+38dup MANE Select	ENSP00000498499.1:n.2669+37_2669+38dup
ENST00000315684.12:c.2669+37_2669+38dup	ENSP00000313759.8:n.2669+37_2669+38dup
ENST00000449476.6:c.2564+37_2564+38dup	ENSP00000396018.2:n.2564+37_2564+38dup
ENST00000578240.1:n.897+37_897+38dup
ENST00000578441.5:n.170+37_170+38dup
ENST00000578537.1:c.371+487_371+488dup
NM_025099.5:c.2669+37_2669+38dup	NP_079375.3:n.2669+37_2669+38dup
NR_046431.1:n.2623+37_2623+38dup
XM_006721577.2:c.2540+37_2540+38dup	XP_006721640.1:n.2540+37_2540+38dup
XM_006721578.2:c.2669+37_2669+38dup	XP_006721641.1:n.2669+37_2669+38dup
XM_006721579.2:c.2669+37_2669+38dup	XP_006721642.1:n.2669+37_2669+38dup
XM_011524010.1:c.2564+37_2564+38dup	XP_011522312.1:n.2564+37_2564+38dup
XM_011524011.1:c.1772+37_1772+38dup	XP_011522313.1:n.1772+37_1772+38dup
XR_429823.2:n.2712+37_2712+38dup
XR_429824.2:n.2712+37_2712+38dup
XR_429825.1:n.2518+487_2518+488dup
NM_025099.6:c.2669+37_2669+38dup MANE Select	NP_079375.3:n.2669+37_2669+38dup
XM_006721577.3:c.2540+37_2540+38dup	XP_006721640.1:n.2540+37_2540+38dup
XM_006721578.3:c.2669+37_2669+38dup	XP_006721641.1:n.2669+37_2669+38dup
XM_011524010.2:c.2564+37_2564+38dup	XP_011522312.1:n.2564+37_2564+38dup
XM_011524011.2:c.1772+37_1772+38dup	XP_011522313.1:n.1772+37_1772+38dup
XR_001752639.1:n.2583+37_2583+38dup
XR_001752640.1:n.2712+37_2712+38dup
XR_001752641.1:n.2712+37_2712+38dup
XR_001752642.1:n.2518+487_2518+488dup
XR_001752643.1:n.3142+37_3142+38dup
XR_002958073.1:n.2518+487_2518+488dup
XR_429823.3:n.2712+37_2712+38dup
XR_429824.3:n.2712+37_2712+38dup
NR_046431.2:n.2584+37_2584+38dup