Canonical Allele Identifier: CA397976560

Gene: CTC1

Linked Data

• MyVariant Identifiers: chr17:g.8135059T>C (hg19) ; chr17:g.8231741T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8231741T>C , CM000679.2:g.8231741T>C	GRCh38
NC_000017.10:g.8135059T>C , CM000679.1:g.8135059T>C	GRCh37
NC_000017.9:g.8075784T>C	NCBI36
NG_032148.1:g.21355A>G
NG_032148.2:g.21355A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000580299.2:c.2460A>G	ENSP00000462607.2:p.Ile820Met
ENST00000581729.2:c.2460A>G	ENSP00000462720.2:p.Ile820Met
ENST00000581967.2:n.2912A>G
ENST00000583254.2:n.3253A>G
ENST00000699849.1:c.1563A>G	ENSP00000514647.1:p.Ile521Met
ENST00000699850.1:n.1723A>G
ENST00000699851.1:n.2482A>G
ENST00000699852.1:c.*1136A>G	ENSP00000514648.1:n.*1136A>G
ENST00000699853.1:c.2460A>G	ENSP00000514649.1:p.Ile820Met
ENST00000699854.1:n.2253A>G
ENST00000699855.1:n.2912A>G
ENST00000699856.1:c.2460A>G	ENSP00000514650.1:p.Ile820Met
ENST00000699857.1:n.2468A>G
ENST00000699858.1:c.*1073A>G	ENSP00000514651.1:n.*1073A>G
ENST00000699859.1:c.2331A>G	ENSP00000514652.1:p.Ile777Met
ENST00000699860.1:n.566A>G
ENST00000699861.1:n.2482A>G
ENST00000699862.1:n.3420A>G
ENST00000449476.7:c.2355A>G	ENSP00000396018.2:p.Ile785Met
ENST00000581671.2:n.2449A>G
ENST00000643543.1:c.*1167A>G	ENSP00000494323.1:n.*1167A>G
ENST00000651323.1:c.2460A>G MANE Select	ENSP00000498499.1:p.Ile820Met
ENST00000315684.12:c.2460A>G	ENSP00000313759.8:p.Ile820Met
ENST00000449476.6:c.2355A>G	ENSP00000396018.2:p.Ile785Met
ENST00000578240.1:n.688A>G
ENST00000578537.1:c.356A>G
NM_025099.5:c.2460A>G	NP_079375.3:p.Ile820Met
NR_046431.1:n.2414A>G
XM_006721577.2:c.2331A>G	XP_006721640.1:p.Ile777Met
XM_006721578.2:c.2460A>G	XP_006721641.1:p.Ile820Met
XM_006721579.2:c.2460A>G	XP_006721642.1:p.Ile820Met
XM_011524010.1:c.2355A>G	XP_011522312.1:p.Ile785Met
XM_011524011.1:c.1563A>G	XP_011522313.1:p.Ile521Met
XR_429823.2:n.2503A>G
XR_429824.2:n.2503A>G
XR_429825.1:n.2503A>G
NM_025099.6:c.2460A>G MANE Select	NP_079375.3:p.Ile820Met
XM_006721577.3:c.2331A>G	XP_006721640.1:p.Ile777Met
XM_006721578.3:c.2460A>G	XP_006721641.1:p.Ile820Met
XM_011524010.2:c.2355A>G	XP_011522312.1:p.Ile785Met
XM_011524011.2:c.1563A>G	XP_011522313.1:p.Ile521Met
XR_001752639.1:n.2374A>G
XR_001752640.1:n.2503A>G
XR_001752641.1:n.2503A>G
XR_001752642.1:n.2503A>G
XR_001752643.1:n.2933A>G
XR_002958073.1:n.2503A>G
XR_429823.3:n.2503A>G
XR_429824.3:n.2503A>G
NR_046431.2:n.2375A>G