Canonical Allele Identifier: CA397978344

Gene: CTC1

Linked Data

• gnomAD v4: 17-8232085-G-A
• MyVariant Identifiers: chr17:g.8135403G>A (hg19) ; chr17:g.8232085G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8232085G>A , CM000679.2:g.8232085G>A	GRCh38
NC_000017.10:g.8135403G>A , CM000679.1:g.8135403G>A	GRCh37
NC_000017.9:g.8076128G>A	NCBI36
NG_032148.1:g.21011C>T
NG_032148.2:g.21011C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000580299.2:c.2203C>T	ENSP00000462607.2:p.Leu735Phe
ENST00000581729.2:c.2203C>T	ENSP00000462720.2:p.Leu735Phe
ENST00000581967.2:n.2655C>T
ENST00000583254.2:n.2909C>T
ENST00000699849.1:c.1306C>T	ENSP00000514647.1:p.Leu436Phe
ENST00000699850.1:n.1466C>T
ENST00000699851.1:n.2225C>T
ENST00000699852.1:c.*879C>T	ENSP00000514648.1:n.*879C>T
ENST00000699853.1:c.2203C>T	ENSP00000514649.1:p.Leu735Phe
ENST00000699854.1:n.1996C>T
ENST00000699855.1:n.2655C>T
ENST00000699856.1:c.2203C>T	ENSP00000514650.1:p.Leu735Phe
ENST00000699857.1:n.2211C>T
ENST00000699858.1:c.*816C>T	ENSP00000514651.1:n.*816C>T
ENST00000699859.1:c.2074C>T	ENSP00000514652.1:p.Leu692Phe
ENST00000699860.1:n.309C>T
ENST00000699861.1:n.2225C>T
ENST00000699862.1:n.3163C>T
ENST00000449476.7:c.2098C>T	ENSP00000396018.2:p.Leu700Phe
ENST00000581671.2:n.2192C>T
ENST00000643543.1:c.*910C>T	ENSP00000494323.1:n.*910C>T
ENST00000651323.1:c.2203C>T MANE Select	ENSP00000498499.1:p.Leu735Phe
ENST00000315684.12:c.2203C>T	ENSP00000313759.8:p.Leu735Phe
ENST00000449476.6:c.2098C>T	ENSP00000396018.2:p.Leu700Phe
ENST00000578240.1:n.431C>T
ENST00000578537.1:c.99C>T
NM_025099.5:c.2203C>T	NP_079375.3:p.Leu735Phe
NR_046431.1:n.2157C>T
XM_006721577.2:c.2074C>T	XP_006721640.1:p.Leu692Phe
XM_006721578.2:c.2203C>T	XP_006721641.1:p.Leu735Phe
XM_006721579.2:c.2203C>T	XP_006721642.1:p.Leu735Phe
XM_011524010.1:c.2098C>T	XP_011522312.1:p.Leu700Phe
XM_011524011.1:c.1306C>T	XP_011522313.1:p.Leu436Phe
XR_429823.2:n.2246C>T
XR_429824.2:n.2246C>T
XR_429825.1:n.2246C>T
NM_025099.6:c.2203C>T MANE Select	NP_079375.3:p.Leu735Phe
XM_006721577.3:c.2074C>T	XP_006721640.1:p.Leu692Phe
XM_006721578.3:c.2203C>T	XP_006721641.1:p.Leu735Phe
XM_011524010.2:c.2098C>T	XP_011522312.1:p.Leu700Phe
XM_011524011.2:c.1306C>T	XP_011522313.1:p.Leu436Phe
XR_001752639.1:n.2117C>T
XR_001752640.1:n.2246C>T
XR_001752641.1:n.2246C>T
XR_001752642.1:n.2246C>T
XR_001752643.1:n.2676C>T
XR_002958073.1:n.2246C>T
XR_429823.3:n.2246C>T
XR_429824.3:n.2246C>T
NR_046431.2:n.2118C>T