Canonical Allele Identifier: CA497959244

Gene: CTC1

Linked Data

• dbSNP Id: rs1177408371
• gnomAD v2: 17-8135500-C-T
• MyVariant Identifiers: chr17:g.8135500C>T (hg19) ; chr17:g.8232182C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8232182C>T , CM000679.2:g.8232182C>T	GRCh38
NC_000017.10:g.8135500C>T , CM000679.1:g.8135500C>T	GRCh37
NC_000017.9:g.8076225C>T	NCBI36
NG_032148.1:g.20914G>A
NG_032148.2:g.20914G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000580299.2:c.2106G>A	ENSP00000462607.2:p.Val702=
ENST00000581729.2:c.2106G>A	ENSP00000462720.2:p.Val702=
ENST00000581967.2:n.2558G>A
ENST00000583254.2:n.2812G>A
ENST00000699849.1:c.1209G>A	ENSP00000514647.1:p.Val403=
ENST00000699850.1:n.1369G>A
ENST00000699851.1:n.2128G>A
ENST00000699852.1:c.*782G>A	ENSP00000514648.1:n.*782G>A
ENST00000699853.1:c.2106G>A	ENSP00000514649.1:p.Val702=
ENST00000699854.1:n.1899G>A
ENST00000699855.1:n.2558G>A
ENST00000699856.1:c.2106G>A	ENSP00000514650.1:p.Val702=
ENST00000699857.1:n.2114G>A
ENST00000699858.1:c.*719G>A	ENSP00000514651.1:n.*719G>A
ENST00000699859.1:c.1977G>A	ENSP00000514652.1:p.Val659=
ENST00000699860.1:n.212G>A
ENST00000699861.1:n.2128G>A
ENST00000699862.1:n.3066G>A
ENST00000449476.7:c.2001G>A	ENSP00000396018.2:p.Val667=
ENST00000581671.2:n.2095G>A
ENST00000643543.1:c.*813G>A	ENSP00000494323.1:n.*813G>A
ENST00000651323.1:c.2106G>A MANE Select	ENSP00000498499.1:p.Val702=
ENST00000315684.12:c.2106G>A	ENSP00000313759.8:p.Val702=
ENST00000449476.6:c.2001G>A	ENSP00000396018.2:p.Val667=
ENST00000578240.1:n.334G>A
ENST00000578537.1:c.2G>A
NM_025099.5:c.2106G>A	NP_079375.3:p.Val702=
NR_046431.1:n.2060G>A
XM_006721577.2:c.1977G>A	XP_006721640.1:p.Val659=
XM_006721578.2:c.2106G>A	XP_006721641.1:p.Val702=
XM_006721579.2:c.2106G>A	XP_006721642.1:p.Val702=
XM_011524010.1:c.2001G>A	XP_011522312.1:p.Val667=
XM_011524011.1:c.1209G>A	XP_011522313.1:p.Val403=
XR_429823.2:n.2149G>A
XR_429824.2:n.2149G>A
XR_429825.1:n.2149G>A
NM_025099.6:c.2106G>A MANE Select	NP_079375.3:p.Val702=
XM_006721577.3:c.1977G>A	XP_006721640.1:p.Val659=
XM_006721578.3:c.2106G>A	XP_006721641.1:p.Val702=
XM_011524010.2:c.2001G>A	XP_011522312.1:p.Val667=
XM_011524011.2:c.1209G>A	XP_011522313.1:p.Val403=
XR_001752639.1:n.2020G>A
XR_001752640.1:n.2149G>A
XR_001752641.1:n.2149G>A
XR_001752642.1:n.2149G>A
XR_001752643.1:n.2579G>A
XR_002958073.1:n.2149G>A
XR_429823.3:n.2149G>A
XR_429824.3:n.2149G>A
NR_046431.2:n.2021G>A