Canonical Allele Identifier: CA397979085

Gene: CTC1

Linked Data

• dbSNP Id: rs1284999014
• gnomAD v4: 17-8232198-G-T
• MyVariant Identifiers: chr17:g.8135516G>T (hg19) ; chr17:g.8232198G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8232198G>T , CM000679.2:g.8232198G>T	GRCh38
NC_000017.10:g.8135516G>T , CM000679.1:g.8135516G>T	GRCh37
NC_000017.9:g.8076241G>T	NCBI36
NG_032148.1:g.20898C>A
NG_032148.2:g.20898C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000580299.2:c.2090C>A	ENSP00000462607.2:p.Ala697Asp
ENST00000581729.2:c.2090C>A	ENSP00000462720.2:p.Ala697Asp
ENST00000581967.2:n.2542C>A
ENST00000583254.2:n.2796C>A
ENST00000699849.1:c.1193C>A	ENSP00000514647.1:p.Ala398Asp
ENST00000699850.1:n.1353C>A
ENST00000699851.1:n.2112C>A
ENST00000699852.1:c.*766C>A	ENSP00000514648.1:n.*766C>A
ENST00000699853.1:c.2090C>A	ENSP00000514649.1:p.Ala697Asp
ENST00000699854.1:n.1883C>A
ENST00000699855.1:n.2542C>A
ENST00000699856.1:c.2090C>A	ENSP00000514650.1:p.Ala697Asp
ENST00000699857.1:n.2098C>A
ENST00000699858.1:c.*703C>A	ENSP00000514651.1:n.*703C>A
ENST00000699859.1:c.1961C>A	ENSP00000514652.1:p.Ala654Asp
ENST00000699860.1:n.196C>A
ENST00000699861.1:n.2112C>A
ENST00000699862.1:n.3050C>A
ENST00000449476.7:c.1985C>A	ENSP00000396018.2:p.Ala662Asp
ENST00000581671.2:n.2079C>A
ENST00000643543.1:c.*797C>A	ENSP00000494323.1:n.*797C>A
ENST00000651323.1:c.2090C>A MANE Select	ENSP00000498499.1:p.Ala697Asp
ENST00000315684.12:c.2090C>A	ENSP00000313759.8:p.Ala697Asp
ENST00000449476.6:c.1985C>A	ENSP00000396018.2:p.Ala662Asp
ENST00000578240.1:n.318C>A
NM_025099.5:c.2090C>A	NP_079375.3:p.Ala697Asp
NR_046431.1:n.2044C>A
XM_006721577.2:c.1961C>A	XP_006721640.1:p.Ala654Asp
XM_006721578.2:c.2090C>A	XP_006721641.1:p.Ala697Asp
XM_006721579.2:c.2090C>A	XP_006721642.1:p.Ala697Asp
XM_011524010.1:c.1985C>A	XP_011522312.1:p.Ala662Asp
XM_011524011.1:c.1193C>A	XP_011522313.1:p.Ala398Asp
XR_429823.2:n.2133C>A
XR_429824.2:n.2133C>A
XR_429825.1:n.2133C>A
NM_025099.6:c.2090C>A MANE Select	NP_079375.3:p.Ala697Asp
XM_006721577.3:c.1961C>A	XP_006721640.1:p.Ala654Asp
XM_006721578.3:c.2090C>A	XP_006721641.1:p.Ala697Asp
XM_011524010.2:c.1985C>A	XP_011522312.1:p.Ala662Asp
XM_011524011.2:c.1193C>A	XP_011522313.1:p.Ala398Asp
XR_001752639.1:n.2004C>A
XR_001752640.1:n.2133C>A
XR_001752641.1:n.2133C>A
XR_001752642.1:n.2133C>A
XR_001752643.1:n.2563C>A
XR_002958073.1:n.2133C>A
XR_429823.3:n.2133C>A
XR_429824.3:n.2133C>A
NR_046431.2:n.2005C>A