Canonical Allele Identifier: CA397979418

Gene: CTC1

Linked Data

• ClinVar Variation Id: 1336850
• ClinVar RCV Id: RCV001819336
• dbSNP Id: rs2151510866
• MyVariant Identifiers: chr17:g.8135691T>G (hg19) ; chr17:g.8232373T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8232373T>G , CM000679.2:g.8232373T>G	GRCh38
NC_000017.10:g.8135691T>G , CM000679.1:g.8135691T>G	GRCh37
NC_000017.9:g.8076416T>G	NCBI36
NG_032148.1:g.20723A>C
NG_032148.2:g.20723A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000580299.2:c.2048A>C	ENSP00000462607.2:p.Lys683Thr
ENST00000581729.2:c.2048A>C	ENSP00000462720.2:p.Lys683Thr
ENST00000581967.2:n.2500A>C
ENST00000583254.2:n.2754A>C
ENST00000699849.1:c.1151A>C	ENSP00000514647.1:p.Lys384Thr
ENST00000699850.1:n.1311A>C
ENST00000699851.1:n.2070A>C
ENST00000699852.1:c.*724A>C	ENSP00000514648.1:n.*724A>C
ENST00000699853.1:c.2048A>C	ENSP00000514649.1:p.Lys683Thr
ENST00000699854.1:n.1841A>C
ENST00000699855.1:n.2500A>C
ENST00000699856.1:c.2048A>C	ENSP00000514650.1:p.Lys683Thr
ENST00000699857.1:n.2056A>C
ENST00000699858.1:c.*661A>C	ENSP00000514651.1:n.*661A>C
ENST00000699859.1:c.1919A>C	ENSP00000514652.1:p.Lys640Thr
ENST00000699860.1:n.154A>C
ENST00000699861.1:n.2070A>C
ENST00000699862.1:n.3008A>C
ENST00000449476.7:c.1943A>C	ENSP00000396018.2:p.Lys648Thr
ENST00000581671.2:n.2037A>C
ENST00000643543.1:c.*755A>C	ENSP00000494323.1:n.*755A>C
ENST00000651323.1:c.2048A>C MANE Select	ENSP00000498499.1:p.Lys683Thr
ENST00000315684.12:c.2048A>C	ENSP00000313759.8:p.Lys683Thr
ENST00000449476.6:c.1943A>C	ENSP00000396018.2:p.Lys648Thr
ENST00000578240.1:n.276A>C
NM_025099.5:c.2048A>C	NP_079375.3:p.Lys683Thr
NR_046431.1:n.2002A>C
XM_006721577.2:c.1919A>C	XP_006721640.1:p.Lys640Thr
XM_006721578.2:c.2048A>C	XP_006721641.1:p.Lys683Thr
XM_006721579.2:c.2048A>C	XP_006721642.1:p.Lys683Thr
XM_011524010.1:c.1943A>C	XP_011522312.1:p.Lys648Thr
XM_011524011.1:c.1151A>C	XP_011522313.1:p.Lys384Thr
XR_429823.2:n.2091A>C
XR_429824.2:n.2091A>C
XR_429825.1:n.2091A>C
NM_025099.6:c.2048A>C MANE Select	NP_079375.3:p.Lys683Thr
XM_006721577.3:c.1919A>C	XP_006721640.1:p.Lys640Thr
XM_006721578.3:c.2048A>C	XP_006721641.1:p.Lys683Thr
XM_011524010.2:c.1943A>C	XP_011522312.1:p.Lys648Thr
XM_011524011.2:c.1151A>C	XP_011522313.1:p.Lys384Thr
XR_001752639.1:n.1962A>C
XR_001752640.1:n.2091A>C
XR_001752641.1:n.2091A>C
XR_001752642.1:n.2091A>C
XR_001752643.1:n.2521A>C
XR_002958073.1:n.2091A>C
XR_429823.3:n.2091A>C
XR_429824.3:n.2091A>C
NR_046431.2:n.1963A>C