Canonical Allele Identifier: CA2635986561

Gene: CTC1

Linked Data

• gnomAD v4: 17-8232854-T-TA

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8232855dup , CM000679.2:g.8232855dup	GRCh38
NC_000017.10:g.8136173dup , CM000679.1:g.8136173dup	GRCh37
NC_000017.9:g.8076898dup	NCBI36
NG_032148.1:g.20241dup
NG_032148.2:g.20241dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000580299.2:c.1945+51dup	ENSP00000462607.2:n.1945+51dup
ENST00000581729.2:c.1945+51dup	ENSP00000462720.2:n.1945+51dup
ENST00000581967.2:n.2018dup
ENST00000583254.2:n.2272dup
ENST00000699849.1:c.1048+51dup	ENSP00000514647.1:n.1048+51dup
ENST00000699850.1:n.1208+51dup
ENST00000699851.1:n.1967+51dup
ENST00000699852.1:c.*242dup	ENSP00000514648.1:n.*242dup
ENST00000699853.1:c.1945+51dup	ENSP00000514649.1:n.1945+51dup
ENST00000699854.1:n.1738+51dup
ENST00000699855.1:n.2018dup
ENST00000699856.1:c.1945+51dup	ENSP00000514650.1:n.1945+51dup
ENST00000699857.1:n.1953+51dup
ENST00000699858.1:c.*558+51dup	ENSP00000514651.1:n.*558+51dup
ENST00000699859.1:c.1816+51dup	ENSP00000514652.1:n.1816+51dup
ENST00000699860.1:n.51+51dup
ENST00000699861.1:n.1967+51dup
ENST00000699862.1:n.2526dup
ENST00000449476.7:c.1840+51dup	ENSP00000396018.2:n.1840+51dup
ENST00000581671.2:n.1934+51dup
ENST00000643543.1:c.*652+51dup	ENSP00000494323.1:n.*652+51dup
ENST00000651323.1:c.1945+51dup MANE Select	ENSP00000498499.1:n.1945+51dup
ENST00000315684.12:c.1945+51dup	ENSP00000313759.8:n.1945+51dup
ENST00000449476.6:c.1840+51dup	ENSP00000396018.2:n.1840+51dup
ENST00000581967.1:n.399dup
NM_025099.5:c.1945+51dup	NP_079375.3:n.1945+51dup
NR_046431.1:n.1899+51dup
XM_006721577.2:c.1816+51dup	XP_006721640.1:n.1816+51dup
XM_006721578.2:c.1945+51dup	XP_006721641.1:n.1945+51dup
XM_006721579.2:c.1945+51dup	XP_006721642.1:n.1945+51dup
XM_011524010.1:c.1840+51dup	XP_011522312.1:n.1840+51dup
XM_011524011.1:c.1048+51dup	XP_011522313.1:n.1048+51dup
XR_429823.2:n.1988+51dup
XR_429824.2:n.1988+51dup
XR_429825.1:n.1988+51dup
NM_025099.6:c.1945+51dup MANE Select	NP_079375.3:n.1945+51dup
XM_006721577.3:c.1816+51dup	XP_006721640.1:n.1816+51dup
XM_006721578.3:c.1945+51dup	XP_006721641.1:n.1945+51dup
XM_011524010.2:c.1840+51dup	XP_011522312.1:n.1840+51dup
XM_011524011.2:c.1048+51dup	XP_011522313.1:n.1048+51dup
XR_001752639.1:n.1859+51dup
XR_001752640.1:n.1988+51dup
XR_001752641.1:n.1988+51dup
XR_001752642.1:n.1988+51dup
XR_001752643.1:n.2039dup
XR_001752644.1:n.2039dup
XR_002958073.1:n.1988+51dup
XR_429823.3:n.1988+51dup
XR_429824.3:n.1988+51dup
NR_046431.2:n.1860+51dup