Canonical Allele Identifier: CA397976209

Gene: CTC1

Linked Data

• MyVariant Identifiers: chr17:g.8134754A>C (hg19) ; chr17:g.8231436A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8231436A>C , CM000679.2:g.8231436A>C	GRCh38
NC_000017.10:g.8134754A>C , CM000679.1:g.8134754A>C	GRCh37
NC_000017.9:g.8075479A>C	NCBI36
NG_032148.1:g.21660T>G
NG_032148.2:g.21660T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000580299.2:c.2509T>G	ENSP00000462607.2:p.Cys837Gly
ENST00000581729.2:c.2509T>G	ENSP00000462720.2:p.Cys837Gly
ENST00000581967.2:n.2961T>G
ENST00000583254.2:n.3558T>G
ENST00000699849.1:c.1612T>G	ENSP00000514647.1:p.Cys538Gly
ENST00000699850.1:n.1772T>G
ENST00000699851.1:n.2531T>G
ENST00000699852.1:c.*1185T>G	ENSP00000514648.1:n.*1185T>G
ENST00000699853.1:c.2509T>G	ENSP00000514649.1:p.Cys837Gly
ENST00000699854.1:n.2302T>G
ENST00000699855.1:n.2961T>G
ENST00000699856.1:c.2509T>G	ENSP00000514650.1:p.Cys837Gly
ENST00000699857.1:n.2517T>G
ENST00000699858.1:c.*1122T>G	ENSP00000514651.1:n.*1122T>G
ENST00000699859.1:c.2380T>G	ENSP00000514652.1:p.Cys794Gly
ENST00000699860.1:n.581+290T>G
ENST00000699861.1:n.2531T>G
ENST00000699862.1:n.3469T>G
ENST00000449476.7:c.2404T>G	ENSP00000396018.2:p.Cys802Gly
ENST00000581671.2:n.2498T>G
ENST00000643543.1:c.*1216T>G	ENSP00000494323.1:n.*1216T>G
ENST00000651323.1:c.2509T>G MANE Select	ENSP00000498499.1:p.Cys837Gly
ENST00000315684.12:c.2509T>G	ENSP00000313759.8:p.Cys837Gly
ENST00000449476.6:c.2404T>G	ENSP00000396018.2:p.Cys802Gly
ENST00000578240.1:n.737T>G
ENST00000578441.5:n.10T>G
ENST00000578537.1:c.371+290T>G
NM_025099.5:c.2509T>G	NP_079375.3:p.Cys837Gly
NR_046431.1:n.2463T>G
XM_006721577.2:c.2380T>G	XP_006721640.1:p.Cys794Gly
XM_006721578.2:c.2509T>G	XP_006721641.1:p.Cys837Gly
XM_006721579.2:c.2509T>G	XP_006721642.1:p.Cys837Gly
XM_011524010.1:c.2404T>G	XP_011522312.1:p.Cys802Gly
XM_011524011.1:c.1612T>G	XP_011522313.1:p.Cys538Gly
XR_429823.2:n.2552T>G
XR_429824.2:n.2552T>G
XR_429825.1:n.2518+290T>G
NM_025099.6:c.2509T>G MANE Select	NP_079375.3:p.Cys837Gly
XM_006721577.3:c.2380T>G	XP_006721640.1:p.Cys794Gly
XM_006721578.3:c.2509T>G	XP_006721641.1:p.Cys837Gly
XM_011524010.2:c.2404T>G	XP_011522312.1:p.Cys802Gly
XM_011524011.2:c.1612T>G	XP_011522313.1:p.Cys538Gly
XR_001752639.1:n.2423T>G
XR_001752640.1:n.2552T>G
XR_001752641.1:n.2552T>G
XR_001752642.1:n.2518+290T>G
XR_001752643.1:n.2982T>G
XR_002958073.1:n.2518+290T>G
XR_429823.3:n.2552T>G
XR_429824.3:n.2552T>G
NR_046431.2:n.2424T>G