Canonical Allele Identifier: CA497959107

Gene: CTC1

Linked Data

• MyVariant Identifiers: chr17:g.8135425T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8232107T>G , CM000679.2:g.8232107T>G	GRCh38
NC_000017.10:g.8135425T>G , CM000679.1:g.8135425T>G	GRCh37
NC_000017.9:g.8076150T>G	NCBI36
NG_032148.1:g.20989A>C
NG_032148.2:g.20989A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000580299.2:c.2181A>C	ENSP00000462607.2:p.Leu727=
ENST00000581729.2:c.2181A>C	ENSP00000462720.2:p.Leu727=
ENST00000581967.2:n.2633A>C
ENST00000583254.2:n.2887A>C
ENST00000699849.1:c.1284A>C	ENSP00000514647.1:p.Leu428=
ENST00000699850.1:n.1444A>C
ENST00000699851.1:n.2203A>C
ENST00000699852.1:c.*857A>C	ENSP00000514648.1:n.*857A>C
ENST00000699853.1:c.2181A>C	ENSP00000514649.1:p.Leu727=
ENST00000699854.1:n.1974A>C
ENST00000699855.1:n.2633A>C
ENST00000699856.1:c.2181A>C	ENSP00000514650.1:p.Leu727=
ENST00000699857.1:n.2189A>C
ENST00000699858.1:c.*794A>C	ENSP00000514651.1:n.*794A>C
ENST00000699859.1:c.2052A>C	ENSP00000514652.1:p.Leu684=
ENST00000699860.1:n.287A>C
ENST00000699861.1:n.2203A>C
ENST00000699862.1:n.3141A>C
ENST00000449476.7:c.2076A>C	ENSP00000396018.2:p.Leu692=
ENST00000581671.2:n.2170A>C
ENST00000643543.1:c.*888A>C	ENSP00000494323.1:n.*888A>C
ENST00000651323.1:c.2181A>C MANE Select	ENSP00000498499.1:p.Leu727=
ENST00000315684.12:c.2181A>C	ENSP00000313759.8:p.Leu727=
ENST00000449476.6:c.2076A>C	ENSP00000396018.2:p.Leu692=
ENST00000578240.1:n.409A>C
ENST00000578537.1:c.77A>C
NM_025099.5:c.2181A>C	NP_079375.3:p.Leu727=
NR_046431.1:n.2135A>C
XM_006721577.2:c.2052A>C	XP_006721640.1:p.Leu684=
XM_006721578.2:c.2181A>C	XP_006721641.1:p.Leu727=
XM_006721579.2:c.2181A>C	XP_006721642.1:p.Leu727=
XM_011524010.1:c.2076A>C	XP_011522312.1:p.Leu692=
XM_011524011.1:c.1284A>C	XP_011522313.1:p.Leu428=
XR_429823.2:n.2224A>C
XR_429824.2:n.2224A>C
XR_429825.1:n.2224A>C
NM_025099.6:c.2181A>C MANE Select	NP_079375.3:p.Leu727=
XM_006721577.3:c.2052A>C	XP_006721640.1:p.Leu684=
XM_006721578.3:c.2181A>C	XP_006721641.1:p.Leu727=
XM_011524010.2:c.2076A>C	XP_011522312.1:p.Leu692=
XM_011524011.2:c.1284A>C	XP_011522313.1:p.Leu428=
XR_001752639.1:n.2095A>C
XR_001752640.1:n.2224A>C
XR_001752641.1:n.2224A>C
XR_001752642.1:n.2224A>C
XR_001752643.1:n.2654A>C
XR_002958073.1:n.2224A>C
XR_429823.3:n.2224A>C
XR_429824.3:n.2224A>C
NR_046431.2:n.2096A>C