Canonical Allele Identifier: CA775732866

Gene: CTC1

Linked Data

• dbSNP Id: rs1192128745
• MyVariant Identifiers: chr17:g.8134505_8134506insA (hg19) ; chr17:g.8231187_8231188insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8231188dup , CM000679.2:g.8231188dup	GRCh38
NC_000017.10:g.8134506dup , CM000679.1:g.8134506dup	GRCh37
NC_000017.9:g.8075231dup	NCBI36
NG_032148.1:g.21908dup
NG_032148.2:g.21908dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000580299.2:c.2669+88dup	ENSP00000462607.2:n.2669+88dup
ENST00000581729.2:c.2669+88dup	ENSP00000462720.2:n.2669+88dup
ENST00000581967.2:n.3121+88dup
ENST00000583254.2:n.3806dup
ENST00000699849.1:c.1772+88dup	ENSP00000514647.1:n.1772+88dup
ENST00000699850.1:n.1932+88dup
ENST00000699851.1:n.2691+88dup
ENST00000699852.1:c.*1345+88dup	ENSP00000514648.1:n.*1345+88dup
ENST00000699853.1:c.2669+88dup	ENSP00000514649.1:n.2669+88dup
ENST00000699854.1:n.2462+88dup
ENST00000699855.1:n.3121+88dup
ENST00000699856.1:c.2669+88dup	ENSP00000514650.1:n.2669+88dup
ENST00000699857.1:n.2677+88dup
ENST00000699858.1:c.*1282+88dup	ENSP00000514651.1:n.*1282+88dup
ENST00000699859.1:c.2540+88dup	ENSP00000514652.1:n.2540+88dup
ENST00000699860.1:n.582-537dup
ENST00000699861.1:n.2691+88dup
ENST00000699862.1:n.3629+88dup
ENST00000449476.7:c.2564+88dup	ENSP00000396018.2:n.2564+88dup
ENST00000581671.2:n.2658+88dup
ENST00000643543.1:c.*1376+88dup	ENSP00000494323.1:n.*1376+88dup
ENST00000651323.1:c.2669+88dup MANE Select	ENSP00000498499.1:n.2669+88dup
ENST00000315684.12:c.2669+88dup	ENSP00000313759.8:n.2669+88dup
ENST00000449476.6:c.2564+88dup	ENSP00000396018.2:n.2564+88dup
ENST00000578240.1:n.897+88dup
ENST00000578441.5:n.170+88dup
ENST00000578537.1:c.372-537dup
NM_025099.5:c.2669+88dup	NP_079375.3:n.2669+88dup
NR_046431.1:n.2623+88dup
XM_006721577.2:c.2540+88dup	XP_006721640.1:n.2540+88dup
XM_006721578.2:c.2669+88dup	XP_006721641.1:n.2669+88dup
XM_006721579.2:c.2669+88dup	XP_006721642.1:n.2669+88dup
XM_011524010.1:c.2564+88dup	XP_011522312.1:n.2564+88dup
XM_011524011.1:c.1772+88dup	XP_011522313.1:n.1772+88dup
XR_429823.2:n.2712+88dup
XR_429824.2:n.2712+88dup
XR_429825.1:n.2519-537dup
NM_025099.6:c.2669+88dup MANE Select	NP_079375.3:n.2669+88dup
XM_006721577.3:c.2540+88dup	XP_006721640.1:n.2540+88dup
XM_006721578.3:c.2669+88dup	XP_006721641.1:n.2669+88dup
XM_011524010.2:c.2564+88dup	XP_011522312.1:n.2564+88dup
XM_011524011.2:c.1772+88dup	XP_011522313.1:n.1772+88dup
XR_001752639.1:n.2583+88dup
XR_001752640.1:n.2712+88dup
XR_001752641.1:n.2712+88dup
XR_001752642.1:n.2519-537dup
XR_001752643.1:n.3142+88dup
XR_002958073.1:n.2519-537dup
XR_429823.3:n.2712+88dup
XR_429824.3:n.2712+88dup
NR_046431.2:n.2584+88dup