Canonical Allele Identifier: CA8371758

Gene: CTC1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8228519C>T , CM000679.2:g.8228519C>T	GRCh38
NC_000017.10:g.8131837C>T , CM000679.1:g.8131837C>T	GRCh37
NC_000017.9:g.8072562C>T	NCBI36
NG_032148.1:g.24577G>A
NG_032148.2:g.24577G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000580299.2:c.3234G>A	ENSP00000462607.2:p.Ser1078=
ENST00000581729.2:c.3267G>A	ENSP00000462720.2:p.Ser1089=
ENST00000699849.1:c.2370G>A	ENSP00000514647.1:p.Ser790=
ENST00000699850.1:n.3430G>A
ENST00000699851.1:n.4384G>A
ENST00000699852.1:c.*2011G>A	ENSP00000514648.1:n.*2011G>A
ENST00000699853.1:c.*83G>A	ENSP00000514649.1:n.*83G>A
ENST00000699854.1:n.4057G>A
ENST00000699855.1:n.4621G>A
ENST00000699856.1:c.*449G>A	ENSP00000514650.1:n.*449G>A
ENST00000699857.1:n.4077G>A
ENST00000699858.1:c.*2782G>A	ENSP00000514651.1:n.*2782G>A
ENST00000699859.1:c.*234G>A	ENSP00000514652.1:n.*234G>A
ENST00000699860.1:n.2176G>A
ENST00000699861.1:n.3961G>A
ENST00000449476.7:c.*232G>A	ENSP00000396018.2:n.*232G>A
ENST00000581671.2:n.3487G>A
ENST00000643543.1:c.*2205G>A	ENSP00000494323.1:n.*2205G>A
ENST00000651323.1:c.3498G>A MANE Select	ENSP00000498499.1:p.Ser1166=
ENST00000315684.12:c.3498G>A	ENSP00000313759.8:p.Ser1166=
ENST00000449476.6:c.*232G>A	ENSP00000396018.2:n.*232G>A
ENST00000581729.1:c.215G>A
NM_025099.5:c.3498G>A	NP_079375.3:p.Ser1166=
NR_046431.1:n.3387G>A
XM_006721577.2:c.3369G>A	XP_006721640.1:p.Ser1123=
XM_006721578.2:c.3267G>A	XP_006721641.1:p.Ser1089=
XM_011524010.1:c.3393G>A	XP_011522312.1:p.Ser1131=
XM_011524011.1:c.2601G>A	XP_011522313.1:p.Ser867=
XR_429823.2:n.3375G>A
XR_429824.2:n.3476G>A
NM_025099.6:c.3498G>A MANE Select	NP_079375.3:p.Ser1166=
XM_006721577.3:c.3369G>A	XP_006721640.1:p.Ser1123=
XM_006721578.3:c.3267G>A	XP_006721641.1:p.Ser1089=
XM_011524010.2:c.3393G>A	XP_011522312.1:p.Ser1131=
XM_011524011.2:c.2601G>A	XP_011522313.1:p.Ser867=
XR_001752639.1:n.3349G>A
XR_001752640.1:n.3497G>A
XR_001752641.1:n.3432G>A
XR_001752642.1:n.3282G>A
XR_002958073.1:n.3788G>A
XR_429823.3:n.3375G>A
XR_429824.3:n.3476G>A
NR_046431.2:n.3348G>A