Canonical Allele Identifier: CA397976637

Gene: CTC1

Linked Data

• MyVariant Identifiers: chr17:g.8135073C>T (hg19) ; chr17:g.8231755C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8231755C>T , CM000679.2:g.8231755C>T	GRCh38
NC_000017.10:g.8135073C>T , CM000679.1:g.8135073C>T	GRCh37
NC_000017.9:g.8075798C>T	NCBI36
NG_032148.1:g.21341G>A
NG_032148.2:g.21341G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000580299.2:c.2446G>A	ENSP00000462607.2:p.Val816Met
ENST00000581729.2:c.2446G>A	ENSP00000462720.2:p.Val816Met
ENST00000581967.2:n.2898G>A
ENST00000583254.2:n.3239G>A
ENST00000699849.1:c.1549G>A	ENSP00000514647.1:p.Val517Met
ENST00000699850.1:n.1709G>A
ENST00000699851.1:n.2468G>A
ENST00000699852.1:c.*1122G>A	ENSP00000514648.1:n.*1122G>A
ENST00000699853.1:c.2446G>A	ENSP00000514649.1:p.Val816Met
ENST00000699854.1:n.2239G>A
ENST00000699855.1:n.2898G>A
ENST00000699856.1:c.2446G>A	ENSP00000514650.1:p.Val816Met
ENST00000699857.1:n.2454G>A
ENST00000699858.1:c.*1059G>A	ENSP00000514651.1:n.*1059G>A
ENST00000699859.1:c.2317G>A	ENSP00000514652.1:p.Val773Met
ENST00000699860.1:n.552G>A
ENST00000699861.1:n.2468G>A
ENST00000699862.1:n.3406G>A
ENST00000449476.7:c.2341G>A	ENSP00000396018.2:p.Val781Met
ENST00000581671.2:n.2435G>A
ENST00000643543.1:c.*1153G>A	ENSP00000494323.1:n.*1153G>A
ENST00000651323.1:c.2446G>A MANE Select	ENSP00000498499.1:p.Val816Met
ENST00000315684.12:c.2446G>A	ENSP00000313759.8:p.Val816Met
ENST00000449476.6:c.2341G>A	ENSP00000396018.2:p.Val781Met
ENST00000578240.1:n.674G>A
ENST00000578537.1:c.342G>A
NM_025099.5:c.2446G>A	NP_079375.3:p.Val816Met
NR_046431.1:n.2400G>A
XM_006721577.2:c.2317G>A	XP_006721640.1:p.Val773Met
XM_006721578.2:c.2446G>A	XP_006721641.1:p.Val816Met
XM_006721579.2:c.2446G>A	XP_006721642.1:p.Val816Met
XM_011524010.1:c.2341G>A	XP_011522312.1:p.Val781Met
XM_011524011.1:c.1549G>A	XP_011522313.1:p.Val517Met
XR_429823.2:n.2489G>A
XR_429824.2:n.2489G>A
XR_429825.1:n.2489G>A
NM_025099.6:c.2446G>A MANE Select	NP_079375.3:p.Val816Met
XM_006721577.3:c.2317G>A	XP_006721640.1:p.Val773Met
XM_006721578.3:c.2446G>A	XP_006721641.1:p.Val816Met
XM_011524010.2:c.2341G>A	XP_011522312.1:p.Val781Met
XM_011524011.2:c.1549G>A	XP_011522313.1:p.Val517Met
XR_001752639.1:n.2360G>A
XR_001752640.1:n.2489G>A
XR_001752641.1:n.2489G>A
XR_001752642.1:n.2489G>A
XR_001752643.1:n.2919G>A
XR_002958073.1:n.2489G>A
XR_429823.3:n.2489G>A
XR_429824.3:n.2489G>A
NR_046431.2:n.2361G>A