Canonical Allele Identifier: CA397978500

Gene: CTC1

Linked Data

• dbSNP Id: rs1483843911
• gnomAD v2: 17-8135423-C-T
• gnomAD v4: 17-8232105-C-T
• MyVariant Identifiers: chr17:g.8135423C>T (hg19) ; chr17:g.8232105C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8232105C>T , CM000679.2:g.8232105C>T	GRCh38
NC_000017.10:g.8135423C>T , CM000679.1:g.8135423C>T	GRCh37
NC_000017.9:g.8076148C>T	NCBI36
NG_032148.1:g.20991G>A
NG_032148.2:g.20991G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000580299.2:c.2183G>A	ENSP00000462607.2:p.Gly728Glu
ENST00000581729.2:c.2183G>A	ENSP00000462720.2:p.Gly728Glu
ENST00000581967.2:n.2635G>A
ENST00000583254.2:n.2889G>A
ENST00000699849.1:c.1286G>A	ENSP00000514647.1:p.Gly429Glu
ENST00000699850.1:n.1446G>A
ENST00000699851.1:n.2205G>A
ENST00000699852.1:c.*859G>A	ENSP00000514648.1:n.*859G>A
ENST00000699853.1:c.2183G>A	ENSP00000514649.1:p.Gly728Glu
ENST00000699854.1:n.1976G>A
ENST00000699855.1:n.2635G>A
ENST00000699856.1:c.2183G>A	ENSP00000514650.1:p.Gly728Glu
ENST00000699857.1:n.2191G>A
ENST00000699858.1:c.*796G>A	ENSP00000514651.1:n.*796G>A
ENST00000699859.1:c.2054G>A	ENSP00000514652.1:p.Gly685Glu
ENST00000699860.1:n.289G>A
ENST00000699861.1:n.2205G>A
ENST00000699862.1:n.3143G>A
ENST00000449476.7:c.2078G>A	ENSP00000396018.2:p.Gly693Glu
ENST00000581671.2:n.2172G>A
ENST00000643543.1:c.*890G>A	ENSP00000494323.1:n.*890G>A
ENST00000651323.1:c.2183G>A MANE Select	ENSP00000498499.1:p.Gly728Glu
ENST00000315684.12:c.2183G>A	ENSP00000313759.8:p.Gly728Glu
ENST00000449476.6:c.2078G>A	ENSP00000396018.2:p.Gly693Glu
ENST00000578240.1:n.411G>A
ENST00000578537.1:c.79G>A
NM_025099.5:c.2183G>A	NP_079375.3:p.Gly728Glu
NR_046431.1:n.2137G>A
XM_006721577.2:c.2054G>A	XP_006721640.1:p.Gly685Glu
XM_006721578.2:c.2183G>A	XP_006721641.1:p.Gly728Glu
XM_006721579.2:c.2183G>A	XP_006721642.1:p.Gly728Glu
XM_011524010.1:c.2078G>A	XP_011522312.1:p.Gly693Glu
XM_011524011.1:c.1286G>A	XP_011522313.1:p.Gly429Glu
XR_429823.2:n.2226G>A
XR_429824.2:n.2226G>A
XR_429825.1:n.2226G>A
NM_025099.6:c.2183G>A MANE Select	NP_079375.3:p.Gly728Glu
XM_006721577.3:c.2054G>A	XP_006721640.1:p.Gly685Glu
XM_006721578.3:c.2183G>A	XP_006721641.1:p.Gly728Glu
XM_011524010.2:c.2078G>A	XP_011522312.1:p.Gly693Glu
XM_011524011.2:c.1286G>A	XP_011522313.1:p.Gly429Glu
XR_001752639.1:n.2097G>A
XR_001752640.1:n.2226G>A
XR_001752641.1:n.2226G>A
XR_001752642.1:n.2226G>A
XR_001752643.1:n.2656G>A
XR_002958073.1:n.2226G>A
XR_429823.3:n.2226G>A
XR_429824.3:n.2226G>A
NR_046431.2:n.2098G>A