Canonical Allele Identifier: CA8371957

Gene: CTC1

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8230401dup , CM000679.2:g.8230401dup	GRCh38
NC_000017.10:g.8133719dup , CM000679.1:g.8133719dup	GRCh37
NC_000017.9:g.8074444dup	NCBI36
NG_032148.1:g.22700dup
NG_032148.2:g.22700dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000580299.2:c.2831dup	ENSP00000462607.2:p.His945SerfsTer?
ENST00000581729.2:c.2831dup	ENSP00000462720.2:p.His945SerfsTer?
ENST00000581967.2:n.3283dup
ENST00000583254.2:n.4504dup
ENST00000699849.1:c.1934dup	ENSP00000514647.1:p.His646SerfsTer?
ENST00000699850.1:n.2094dup
ENST00000699851.1:n.2853dup
ENST00000699852.1:c.*1457-48dup	ENSP00000514648.1:n.*1457-48dup
ENST00000699853.1:c.2831dup	ENSP00000514649.1:p.His945SerfsTer?
ENST00000699854.1:n.2624dup
ENST00000699855.1:n.3283dup
ENST00000699856.1:c.2831dup	ENSP00000514650.1:p.His945SerfsTer?
ENST00000699857.1:n.2789-48dup
ENST00000699858.1:c.*1444dup	ENSP00000514651.1:n.*1444dup
ENST00000699859.1:c.2702dup	ENSP00000514652.1:p.His902SerfsTer?
ENST00000699860.1:n.743dup
ENST00000699861.1:n.2853dup
ENST00000699862.1:n.3791dup
ENST00000449476.7:c.2726dup	ENSP00000396018.2:p.His910SerfsTer?
ENST00000581671.2:n.2820dup
ENST00000643543.1:c.*1538dup	ENSP00000494323.1:n.*1538dup
ENST00000651323.1:c.2831dup MANE Select	ENSP00000498499.1:p.His945SerfsTer?
ENST00000315684.12:c.2831dup	ENSP00000313759.8:p.His945SerfsTer?
ENST00000449476.6:c.2726dup	ENSP00000396018.2:p.His910SerfsTer?
ENST00000578240.1:n.1059dup
ENST00000578441.5:n.282-48dup
ENST00000578537.1:c.533dup
ENST00000584439.1:n.444dup
NM_025099.5:c.2831dup	NP_079375.3:p.His945SerfsTer?
NR_046431.1:n.2785dup
XM_006721577.2:c.2702dup	XP_006721640.1:p.His902SerfsTer?
XM_006721578.2:c.2831dup	XP_006721641.1:p.His945SerfsTer?
XM_006721579.2:c.2831dup	XP_006721642.1:p.His945SerfsTer?
XM_011524010.1:c.2726dup	XP_011522312.1:p.His910SerfsTer?
XM_011524011.1:c.1934dup	XP_011522313.1:p.His646SerfsTer?
XR_429823.2:n.2874dup
XR_429824.2:n.2874dup
XR_429825.1:n.2680dup
NM_025099.6:c.2831dup MANE Select	NP_079375.3:p.His945SerfsTer?
XM_006721577.3:c.2702dup	XP_006721640.1:p.His902SerfsTer?
XM_006721578.3:c.2831dup	XP_006721641.1:p.His945SerfsTer?
XM_011524010.2:c.2726dup	XP_011522312.1:p.His910SerfsTer?
XM_011524011.2:c.1934dup	XP_011522313.1:p.His646SerfsTer?
XR_001752639.1:n.2745dup
XR_001752640.1:n.2874dup
XR_001752641.1:n.2874dup
XR_001752642.1:n.2680dup
XR_001752643.1:n.3304dup
XR_002958073.1:n.2680dup
XR_429823.3:n.2874dup
XR_429824.3:n.2874dup
NR_046431.2:n.2746dup