Canonical Allele Identifier: CA397968004

Gene: CTC1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8228305G>C , CM000679.2:g.8228305G>C	GRCh38
NC_000017.10:g.8131623G>C , CM000679.1:g.8131623G>C	GRCh37
NC_000017.9:g.8072348G>C	NCBI36
NG_032148.1:g.24791C>G
NG_032148.2:g.24791C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000580299.2:c.3265C>G	ENSP00000462607.2:p.Gln1089Glu
ENST00000581729.2:c.3298C>G	ENSP00000462720.2:p.Gln1100Glu
ENST00000699849.1:c.2401C>G	ENSP00000514647.1:p.Gln801Glu
ENST00000699850.1:n.3461C>G
ENST00000699851.1:n.4415C>G
ENST00000699852.1:c.*2042C>G	ENSP00000514648.1:n.*2042C>G
ENST00000699853.1:c.*114C>G	ENSP00000514649.1:n.*114C>G
ENST00000699854.1:n.4088C>G
ENST00000699855.1:n.4652C>G
ENST00000699856.1:c.*480C>G	ENSP00000514650.1:n.*480C>G
ENST00000699857.1:n.4108C>G
ENST00000699858.1:c.*2813C>G	ENSP00000514651.1:n.*2813C>G
ENST00000699859.1:c.*265C>G	ENSP00000514652.1:n.*265C>G
ENST00000699860.1:n.2207C>G
ENST00000699861.1:n.3992C>G
ENST00000449476.7:c.*263C>G	ENSP00000396018.2:n.*263C>G
ENST00000581671.2:n.3518C>G
ENST00000643543.1:c.*2236C>G	ENSP00000494323.1:n.*2236C>G
ENST00000651323.1:c.3529C>G MANE Select	ENSP00000498499.1:p.Gln1177Glu
ENST00000315684.12:c.3529C>G	ENSP00000313759.8:p.Gln1177Glu
ENST00000449476.6:c.*263C>G	ENSP00000396018.2:n.*263C>G
ENST00000581729.1:c.246C>G
NM_025099.5:c.3529C>G	NP_079375.3:p.Gln1177Glu
NR_046431.1:n.3418C>G
XM_006721577.2:c.3400C>G	XP_006721640.1:p.Gln1134Glu
XM_006721578.2:c.3298C>G	XP_006721641.1:p.Gln1100Glu
XM_011524010.1:c.3424C>G	XP_011522312.1:p.Gln1142Glu
XM_011524011.1:c.2632C>G	XP_011522313.1:p.Gln878Glu
XR_429823.2:n.3406C>G
XR_429824.2:n.3507C>G
NM_025099.6:c.3529C>G MANE Select	NP_079375.3:p.Gln1177Glu
XM_006721577.3:c.3400C>G	XP_006721640.1:p.Gln1134Glu
XM_006721578.3:c.3298C>G	XP_006721641.1:p.Gln1100Glu
XM_011524010.2:c.3424C>G	XP_011522312.1:p.Gln1142Glu
XM_011524011.2:c.2632C>G	XP_011522313.1:p.Gln878Glu
XR_001752639.1:n.3380C>G
XR_001752640.1:n.3528C>G
XR_001752641.1:n.3463C>G
XR_001752642.1:n.3313C>G
XR_002958073.1:n.3819C>G
XR_429823.3:n.3406C>G
XR_429824.3:n.3507C>G
NR_046431.2:n.3379C>G