Canonical Allele Identifier: CA397978374

Gene: CTC1

Linked Data

• gnomAD v4: 17-8232089-G-C
• MyVariant Identifiers: chr17:g.8135407G>C (hg19) ; chr17:g.8232089G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8232089G>C , CM000679.2:g.8232089G>C	GRCh38
NC_000017.10:g.8135407G>C , CM000679.1:g.8135407G>C	GRCh37
NC_000017.9:g.8076132G>C	NCBI36
NG_032148.1:g.21007C>G
NG_032148.2:g.21007C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000580299.2:c.2199C>G	ENSP00000462607.2:p.Phe733Leu
ENST00000581729.2:c.2199C>G	ENSP00000462720.2:p.Phe733Leu
ENST00000581967.2:n.2651C>G
ENST00000583254.2:n.2905C>G
ENST00000699849.1:c.1302C>G	ENSP00000514647.1:p.Phe434Leu
ENST00000699850.1:n.1462C>G
ENST00000699851.1:n.2221C>G
ENST00000699852.1:c.*875C>G	ENSP00000514648.1:n.*875C>G
ENST00000699853.1:c.2199C>G	ENSP00000514649.1:p.Phe733Leu
ENST00000699854.1:n.1992C>G
ENST00000699855.1:n.2651C>G
ENST00000699856.1:c.2199C>G	ENSP00000514650.1:p.Phe733Leu
ENST00000699857.1:n.2207C>G
ENST00000699858.1:c.*812C>G	ENSP00000514651.1:n.*812C>G
ENST00000699859.1:c.2070C>G	ENSP00000514652.1:p.Phe690Leu
ENST00000699860.1:n.305C>G
ENST00000699861.1:n.2221C>G
ENST00000699862.1:n.3159C>G
ENST00000449476.7:c.2094C>G	ENSP00000396018.2:p.Phe698Leu
ENST00000581671.2:n.2188C>G
ENST00000643543.1:c.*906C>G	ENSP00000494323.1:n.*906C>G
ENST00000651323.1:c.2199C>G MANE Select	ENSP00000498499.1:p.Phe733Leu
ENST00000315684.12:c.2199C>G	ENSP00000313759.8:p.Phe733Leu
ENST00000449476.6:c.2094C>G	ENSP00000396018.2:p.Phe698Leu
ENST00000578240.1:n.427C>G
ENST00000578537.1:c.95C>G
NM_025099.5:c.2199C>G	NP_079375.3:p.Phe733Leu
NR_046431.1:n.2153C>G
XM_006721577.2:c.2070C>G	XP_006721640.1:p.Phe690Leu
XM_006721578.2:c.2199C>G	XP_006721641.1:p.Phe733Leu
XM_006721579.2:c.2199C>G	XP_006721642.1:p.Phe733Leu
XM_011524010.1:c.2094C>G	XP_011522312.1:p.Phe698Leu
XM_011524011.1:c.1302C>G	XP_011522313.1:p.Phe434Leu
XR_429823.2:n.2242C>G
XR_429824.2:n.2242C>G
XR_429825.1:n.2242C>G
NM_025099.6:c.2199C>G MANE Select	NP_079375.3:p.Phe733Leu
XM_006721577.3:c.2070C>G	XP_006721640.1:p.Phe690Leu
XM_006721578.3:c.2199C>G	XP_006721641.1:p.Phe733Leu
XM_011524010.2:c.2094C>G	XP_011522312.1:p.Phe698Leu
XM_011524011.2:c.1302C>G	XP_011522313.1:p.Phe434Leu
XR_001752639.1:n.2113C>G
XR_001752640.1:n.2242C>G
XR_001752641.1:n.2242C>G
XR_001752642.1:n.2242C>G
XR_001752643.1:n.2672C>G
XR_002958073.1:n.2242C>G
XR_429823.3:n.2242C>G
XR_429824.3:n.2242C>G
NR_046431.2:n.2114C>G