Canonical Allele Identifier: CA397979882

Gene: CTC1

Linked Data

• MyVariant Identifiers: chr17:g.8135754T>A (hg19) ; chr17:g.8232436T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8232436T>A , CM000679.2:g.8232436T>A	GRCh38
NC_000017.10:g.8135754T>A , CM000679.1:g.8135754T>A	GRCh37
NC_000017.9:g.8076479T>A	NCBI36
NG_032148.1:g.20660A>T
NG_032148.2:g.20660A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000580299.2:c.1985A>T	ENSP00000462607.2:p.Glu662Val
ENST00000581729.2:c.1985A>T	ENSP00000462720.2:p.Glu662Val
ENST00000581967.2:n.2437A>T
ENST00000583254.2:n.2691A>T
ENST00000699849.1:c.1088A>T	ENSP00000514647.1:p.Glu363Val
ENST00000699850.1:n.1248A>T
ENST00000699851.1:n.2007A>T
ENST00000699852.1:c.*661A>T	ENSP00000514648.1:n.*661A>T
ENST00000699853.1:c.1985A>T	ENSP00000514649.1:p.Glu662Val
ENST00000699854.1:n.1778A>T
ENST00000699855.1:n.2437A>T
ENST00000699856.1:c.1985A>T	ENSP00000514650.1:p.Glu662Val
ENST00000699857.1:n.1993A>T
ENST00000699858.1:c.*598A>T	ENSP00000514651.1:n.*598A>T
ENST00000699859.1:c.1856A>T	ENSP00000514652.1:p.Glu619Val
ENST00000699860.1:n.91A>T
ENST00000699861.1:n.2007A>T
ENST00000699862.1:n.2945A>T
ENST00000449476.7:c.1880A>T	ENSP00000396018.2:p.Glu627Val
ENST00000581671.2:n.1974A>T
ENST00000643543.1:c.*692A>T	ENSP00000494323.1:n.*692A>T
ENST00000651323.1:c.1985A>T MANE Select	ENSP00000498499.1:p.Glu662Val
ENST00000315684.12:c.1985A>T	ENSP00000313759.8:p.Glu662Val
ENST00000449476.6:c.1880A>T	ENSP00000396018.2:p.Glu627Val
ENST00000578240.1:n.213A>T
NM_025099.5:c.1985A>T	NP_079375.3:p.Glu662Val
NR_046431.1:n.1939A>T
XM_006721577.2:c.1856A>T	XP_006721640.1:p.Glu619Val
XM_006721578.2:c.1985A>T	XP_006721641.1:p.Glu662Val
XM_006721579.2:c.1985A>T	XP_006721642.1:p.Glu662Val
XM_011524010.1:c.1880A>T	XP_011522312.1:p.Glu627Val
XM_011524011.1:c.1088A>T	XP_011522313.1:p.Glu363Val
XR_429823.2:n.2028A>T
XR_429824.2:n.2028A>T
XR_429825.1:n.2028A>T
NM_025099.6:c.1985A>T MANE Select	NP_079375.3:p.Glu662Val
XM_006721577.3:c.1856A>T	XP_006721640.1:p.Glu619Val
XM_006721578.3:c.1985A>T	XP_006721641.1:p.Glu662Val
XM_011524010.2:c.1880A>T	XP_011522312.1:p.Glu627Val
XM_011524011.2:c.1088A>T	XP_011522313.1:p.Glu363Val
XR_001752639.1:n.1899A>T
XR_001752640.1:n.2028A>T
XR_001752641.1:n.2028A>T
XR_001752642.1:n.2028A>T
XR_001752643.1:n.2458A>T
XR_001752644.1:n.2314A>T
XR_002958073.1:n.2028A>T
XR_429823.3:n.2028A>T
XR_429824.3:n.2028A>T
NR_046431.2:n.1900A>T