Canonical Allele Identifier: CA8372079

Gene: CTC1

Linked Data

• ClinVar Variation Id: 962793
• ClinVar RCV Id: RCV001236715
• dbSNP Id: rs772328631
• ExAC: 17:8135066 C / A
• gnomAD v2: 17-8135066-C-A
• gnomAD v4: 17-8231748-C-A
• MyVariant Identifiers: chr17:g.8135066C>A (hg19) ; chr17:g.8231748C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8231748C>A , CM000679.2:g.8231748C>A	GRCh38
NC_000017.10:g.8135066C>A , CM000679.1:g.8135066C>A	GRCh37
NC_000017.9:g.8075791C>A	NCBI36
NG_032148.1:g.21348G>T
NG_032148.2:g.21348G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000580299.2:c.2453G>T	ENSP00000462607.2:p.Arg818Leu
ENST00000581729.2:c.2453G>T	ENSP00000462720.2:p.Arg818Leu
ENST00000581967.2:n.2905G>T
ENST00000583254.2:n.3246G>T
ENST00000699849.1:c.1556G>T	ENSP00000514647.1:p.Arg519Leu
ENST00000699850.1:n.1716G>T
ENST00000699851.1:n.2475G>T
ENST00000699852.1:c.*1129G>T	ENSP00000514648.1:n.*1129G>T
ENST00000699853.1:c.2453G>T	ENSP00000514649.1:p.Arg818Leu
ENST00000699854.1:n.2246G>T
ENST00000699855.1:n.2905G>T
ENST00000699856.1:c.2453G>T	ENSP00000514650.1:p.Arg818Leu
ENST00000699857.1:n.2461G>T
ENST00000699858.1:c.*1066G>T	ENSP00000514651.1:n.*1066G>T
ENST00000699859.1:c.2324G>T	ENSP00000514652.1:p.Arg775Leu
ENST00000699860.1:n.559G>T
ENST00000699861.1:n.2475G>T
ENST00000699862.1:n.3413G>T
ENST00000449476.7:c.2348G>T	ENSP00000396018.2:p.Arg783Leu
ENST00000581671.2:n.2442G>T
ENST00000643543.1:c.*1160G>T	ENSP00000494323.1:n.*1160G>T
ENST00000651323.1:c.2453G>T MANE Select	ENSP00000498499.1:p.Arg818Leu
ENST00000315684.12:c.2453G>T	ENSP00000313759.8:p.Arg818Leu
ENST00000449476.6:c.2348G>T	ENSP00000396018.2:p.Arg783Leu
ENST00000578240.1:n.681G>T
ENST00000578537.1:c.349G>T
NM_025099.5:c.2453G>T	NP_079375.3:p.Arg818Leu
NR_046431.1:n.2407G>T
XM_006721577.2:c.2324G>T	XP_006721640.1:p.Arg775Leu
XM_006721578.2:c.2453G>T	XP_006721641.1:p.Arg818Leu
XM_006721579.2:c.2453G>T	XP_006721642.1:p.Arg818Leu
XM_011524010.1:c.2348G>T	XP_011522312.1:p.Arg783Leu
XM_011524011.1:c.1556G>T	XP_011522313.1:p.Arg519Leu
XR_429823.2:n.2496G>T
XR_429824.2:n.2496G>T
XR_429825.1:n.2496G>T
NM_025099.6:c.2453G>T MANE Select	NP_079375.3:p.Arg818Leu
XM_006721577.3:c.2324G>T	XP_006721640.1:p.Arg775Leu
XM_006721578.3:c.2453G>T	XP_006721641.1:p.Arg818Leu
XM_011524010.2:c.2348G>T	XP_011522312.1:p.Arg783Leu
XM_011524011.2:c.1556G>T	XP_011522313.1:p.Arg519Leu
XR_001752639.1:n.2367G>T
XR_001752640.1:n.2496G>T
XR_001752641.1:n.2496G>T
XR_001752642.1:n.2496G>T
XR_001752643.1:n.2926G>T
XR_002958073.1:n.2496G>T
XR_429823.3:n.2496G>T
XR_429824.3:n.2496G>T
NR_046431.2:n.2368G>T