Canonical Allele Identifier: CA2246176605

Gene: CTC1

Linked Data

• dbSNP Id: rs1987356656
• gnomAD v4: 17-8232784-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8232784T>G , CM000679.2:g.8232784T>G	GRCh38
NC_000017.10:g.8136102T>G , CM000679.1:g.8136102T>G	GRCh37
NC_000017.9:g.8076827T>G	NCBI36
NG_032148.1:g.20312A>C
NG_032148.2:g.20312A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000580299.2:c.1945+122A>C	ENSP00000462607.2:n.1945+122A>C
ENST00000581729.2:c.1945+122A>C	ENSP00000462720.2:n.1945+122A>C
ENST00000581967.2:n.2089A>C
ENST00000583254.2:n.2343A>C
ENST00000699849.1:c.1048+122A>C	ENSP00000514647.1:n.1048+122A>C
ENST00000699850.1:n.1208+122A>C
ENST00000699851.1:n.1967+122A>C
ENST00000699852.1:c.*313A>C	ENSP00000514648.1:n.*313A>C
ENST00000699853.1:c.1945+122A>C	ENSP00000514649.1:n.1945+122A>C
ENST00000699854.1:n.1738+122A>C
ENST00000699855.1:n.2089A>C
ENST00000699856.1:c.1945+122A>C	ENSP00000514650.1:n.1945+122A>C
ENST00000699857.1:n.1953+122A>C
ENST00000699858.1:c.*558+122A>C	ENSP00000514651.1:n.*558+122A>C
ENST00000699859.1:c.1816+122A>C	ENSP00000514652.1:n.1816+122A>C
ENST00000699860.1:n.51+122A>C
ENST00000699861.1:n.1967+122A>C
ENST00000699862.1:n.2597A>C
ENST00000449476.7:c.1840+122A>C	ENSP00000396018.2:n.1840+122A>C
ENST00000581671.2:n.1934+122A>C
ENST00000643543.1:c.*652+122A>C	ENSP00000494323.1:n.*652+122A>C
ENST00000651323.1:c.1945+122A>C MANE Select	ENSP00000498499.1:n.1945+122A>C
ENST00000315684.12:c.1945+122A>C	ENSP00000313759.8:n.1945+122A>C
ENST00000449476.6:c.1840+122A>C	ENSP00000396018.2:n.1840+122A>C
ENST00000581967.1:n.470A>C
NM_025099.5:c.1945+122A>C	NP_079375.3:n.1945+122A>C
NR_046431.1:n.1899+122A>C
XM_006721577.2:c.1816+122A>C	XP_006721640.1:n.1816+122A>C
XM_006721578.2:c.1945+122A>C	XP_006721641.1:n.1945+122A>C
XM_006721579.2:c.1945+122A>C	XP_006721642.1:n.1945+122A>C
XM_011524010.1:c.1840+122A>C	XP_011522312.1:n.1840+122A>C
XM_011524011.1:c.1048+122A>C	XP_011522313.1:n.1048+122A>C
XR_429823.2:n.1988+122A>C
XR_429824.2:n.1988+122A>C
XR_429825.1:n.1988+122A>C
NM_025099.6:c.1945+122A>C MANE Select	NP_079375.3:n.1945+122A>C
XM_006721577.3:c.1816+122A>C	XP_006721640.1:n.1816+122A>C
XM_006721578.3:c.1945+122A>C	XP_006721641.1:n.1945+122A>C
XM_011524010.2:c.1840+122A>C	XP_011522312.1:n.1840+122A>C
XM_011524011.2:c.1048+122A>C	XP_011522313.1:n.1048+122A>C
XR_001752639.1:n.1859+122A>C
XR_001752640.1:n.1988+122A>C
XR_001752641.1:n.1988+122A>C
XR_001752642.1:n.1988+122A>C
XR_001752643.1:n.2110A>C
XR_001752644.1:n.2110A>C
XR_002958073.1:n.1988+122A>C
XR_429823.3:n.1988+122A>C
XR_429824.3:n.1988+122A>C
NR_046431.2:n.1860+122A>C