Canonical Allele Identifier: CA8371767

Gene: CTC1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8228559C>G , CM000679.2:g.8228559C>G	GRCh38
NC_000017.10:g.8131877C>G , CM000679.1:g.8131877C>G	GRCh37
NC_000017.9:g.8072602C>G	NCBI36
NG_032148.1:g.24537G>C
NG_032148.2:g.24537G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000580299.2:c.3194G>C	ENSP00000462607.2:p.Arg1065Pro
ENST00000581729.2:c.3227G>C	ENSP00000462720.2:p.Arg1076Pro
ENST00000699849.1:c.2330G>C	ENSP00000514647.1:p.Arg777Pro
ENST00000699850.1:n.3390G>C
ENST00000699851.1:n.4344G>C
ENST00000699852.1:c.*1971G>C	ENSP00000514648.1:n.*1971G>C
ENST00000699853.1:c.*43G>C	ENSP00000514649.1:n.*43G>C
ENST00000699854.1:n.4017G>C
ENST00000699855.1:n.4581G>C
ENST00000699856.1:c.*409G>C	ENSP00000514650.1:n.*409G>C
ENST00000699857.1:n.4037G>C
ENST00000699858.1:c.*2742G>C	ENSP00000514651.1:n.*2742G>C
ENST00000699859.1:c.*194G>C	ENSP00000514652.1:n.*194G>C
ENST00000699860.1:n.2136G>C
ENST00000699861.1:n.3921G>C
ENST00000449476.7:c.*192G>C	ENSP00000396018.2:n.*192G>C
ENST00000581671.2:n.3447G>C
ENST00000643543.1:c.*2165G>C	ENSP00000494323.1:n.*2165G>C
ENST00000651323.1:c.3458G>C MANE Select	ENSP00000498499.1:p.Arg1153Pro
ENST00000315684.12:c.3458G>C	ENSP00000313759.8:p.Arg1153Pro
ENST00000449476.6:c.*192G>C	ENSP00000396018.2:n.*192G>C
ENST00000580299.1:c.365G>C	ENSP00000462607.1:p.Arg122Pro
ENST00000581729.1:c.175G>C
NM_025099.5:c.3458G>C	NP_079375.3:p.Arg1153Pro
NR_046431.1:n.3347G>C
XM_006721577.2:c.3329G>C	XP_006721640.1:p.Arg1110Pro
XM_006721578.2:c.3227G>C	XP_006721641.1:p.Arg1076Pro
XM_011524010.1:c.3353G>C	XP_011522312.1:p.Arg1118Pro
XM_011524011.1:c.2561G>C	XP_011522313.1:p.Arg854Pro
XR_429823.2:n.3335G>C
XR_429824.2:n.3436G>C
NM_025099.6:c.3458G>C MANE Select	NP_079375.3:p.Arg1153Pro
XM_006721577.3:c.3329G>C	XP_006721640.1:p.Arg1110Pro
XM_006721578.3:c.3227G>C	XP_006721641.1:p.Arg1076Pro
XM_011524010.2:c.3353G>C	XP_011522312.1:p.Arg1118Pro
XM_011524011.2:c.2561G>C	XP_011522313.1:p.Arg854Pro
XR_001752639.1:n.3309G>C
XR_001752640.1:n.3457G>C
XR_001752641.1:n.3392G>C
XR_001752642.1:n.3242G>C
XR_002958073.1:n.3748G>C
XR_429823.3:n.3335G>C
XR_429824.3:n.3436G>C
NR_046431.2:n.3308G>C