Canonical Allele Identifier: CA397984744

Gene: CTC1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8235190G>C , CM000679.2:g.8235190G>C	GRCh38
NC_000017.10:g.8138508G>C , CM000679.1:g.8138508G>C	GRCh37
NC_000017.9:g.8079233G>C	NCBI36
NG_032148.1:g.17906C>G
NG_032148.2:g.17906C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_025099.6:c.1302C>G MANE Select	NP_079375.3:p.Phe434Leu
ENST00000651323.1:c.1302C>G MANE Select	ENSP00000498499.1:p.Phe434Leu
NM_025099.5:c.1302C>G	NP_079375.3:p.Phe434Leu
NR_046431.1:n.1256C>G
NR_046431.2:n.1217C>G
ENST00000315684.12:c.1302C>G	ENSP00000313759.8:p.Phe434Leu
ENST00000449476.6:c.1197C>G	ENSP00000396018.2:p.Phe399Leu
ENST00000449476.7:c.1197C>G	ENSP00000396018.2:p.Phe399Leu
ENST00000579066.1:n.177C>G
ENST00000580299.2:c.1302C>G	ENSP00000462607.2:p.Phe434Leu
ENST00000581671.2:n.1143C>G
ENST00000581729.2:c.1302C>G	ENSP00000462720.2:p.Phe434Leu
ENST00000581967.2:n.1324C>G
ENST00000583254.2:n.1359C>G
ENST00000643543.1:c.1148C>G	ENSP00000494323.1:p.Ser383Cys
ENST00000699849.1:c.405C>G	ENSP00000514647.1:p.Phe135Leu
ENST00000699850.1:n.565C>G
ENST00000699851.1:n.1324C>G
ENST00000699852.1:c.1302C>G	ENSP00000514648.1:p.Phe434Leu
ENST00000699853.1:c.1302C>G	ENSP00000514649.1:p.Phe434Leu
ENST00000699854.1:n.1095C>G
ENST00000699855.1:n.1324C>G
ENST00000699856.1:c.1302C>G	ENSP00000514650.1:p.Phe434Leu
ENST00000699857.1:n.1310C>G
ENST00000699858.1:c.1148C>G	ENSP00000514651.1:p.Ser383Cys
ENST00000699859.1:c.1173C>G	ENSP00000514652.1:p.Phe391Leu
ENST00000699861.1:n.1324C>G
ENST00000699862.1:n.1189C>G
XM_006721577.2:c.1173C>G	XP_006721640.1:p.Phe391Leu
XM_006721577.3:c.1173C>G	XP_006721640.1:p.Phe391Leu
XM_006721578.2:c.1302C>G	XP_006721641.1:p.Phe434Leu
XM_006721578.3:c.1302C>G	XP_006721641.1:p.Phe434Leu
XM_006721579.2:c.1302C>G	XP_006721642.1:p.Phe434Leu
XM_011524010.1:c.1197C>G	XP_011522312.1:p.Phe399Leu
XM_011524010.2:c.1197C>G	XP_011522312.1:p.Phe399Leu
XM_011524011.1:c.405C>G	XP_011522313.1:p.Phe135Leu
XM_011524011.2:c.405C>G	XP_011522313.1:p.Phe135Leu
XR_001752639.1:n.1216C>G
XR_001752640.1:n.1345C>G
XR_001752641.1:n.1345C>G
XR_001752642.1:n.1345C>G
XR_001752643.1:n.1345C>G
XR_001752644.1:n.1345C>G
XR_002958073.1:n.1345C>G
XR_429823.2:n.1345C>G
XR_429823.3:n.1345C>G
XR_429824.2:n.1345C>G
XR_429824.3:n.1345C>G
XR_429825.1:n.1345C>G