Canonical Allele Identifier: CA8371715

Gene: CTC1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8228296G>A , CM000679.2:g.8228296G>A	GRCh38
NC_000017.10:g.8131614G>A , CM000679.1:g.8131614G>A	GRCh37
NC_000017.9:g.8072339G>A	NCBI36
NG_032148.1:g.24800C>T
NG_032148.2:g.24800C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_025099.6:c.3538C>T MANE Select	NP_079375.3:p.Gln1180Ter
ENST00000651323.1:c.3538C>T MANE Select	ENSP00000498499.1:p.Gln1180Ter
NM_025099.5:c.3538C>T	NP_079375.3:p.Gln1180Ter
NR_046431.1:n.3427C>T
NR_046431.2:n.3388C>T
ENST00000315684.12:c.3538C>T	ENSP00000313759.8:p.Gln1180Ter
ENST00000449476.6:c.*272C>T	ENSP00000396018.2:n.*272C>T
ENST00000449476.7:c.*272C>T	ENSP00000396018.2:n.*272C>T
ENST00000580299.2:c.3274C>T	ENSP00000462607.2:p.Gln1092Ter
ENST00000581671.2:n.3527C>T
ENST00000581729.1:c.255C>T
ENST00000581729.2:c.3307C>T	ENSP00000462720.2:p.Gln1103Ter
ENST00000643543.1:c.*2245C>T	ENSP00000494323.1:n.*2245C>T
ENST00000699849.1:c.2410C>T	ENSP00000514647.1:p.Gln804Ter
ENST00000699850.1:n.3470C>T
ENST00000699851.1:n.4424C>T
ENST00000699852.1:c.*2051C>T	ENSP00000514648.1:n.*2051C>T
ENST00000699853.1:c.*123C>T	ENSP00000514649.1:n.*123C>T
ENST00000699854.1:n.4097C>T
ENST00000699855.1:n.4661C>T
ENST00000699856.1:c.*489C>T	ENSP00000514650.1:n.*489C>T
ENST00000699857.1:n.4117C>T
ENST00000699858.1:c.*2822C>T	ENSP00000514651.1:n.*2822C>T
ENST00000699859.1:c.*274C>T	ENSP00000514652.1:n.*274C>T
ENST00000699860.1:n.2216C>T
ENST00000699861.1:n.4001C>T
XM_006721577.2:c.3409C>T	XP_006721640.1:p.Gln1137Ter
XM_006721577.3:c.3409C>T	XP_006721640.1:p.Gln1137Ter
XM_006721578.2:c.3307C>T	XP_006721641.1:p.Gln1103Ter
XM_006721578.3:c.3307C>T	XP_006721641.1:p.Gln1103Ter
XM_011524010.1:c.3433C>T	XP_011522312.1:p.Gln1145Ter
XM_011524010.2:c.3433C>T	XP_011522312.1:p.Gln1145Ter
XM_011524011.1:c.2641C>T	XP_011522313.1:p.Gln881Ter
XM_011524011.2:c.2641C>T	XP_011522313.1:p.Gln881Ter
XR_001752639.1:n.3389C>T
XR_001752640.1:n.3537C>T
XR_001752641.1:n.3472C>T
XR_001752642.1:n.3322C>T
XR_002958073.1:n.3828C>T
XR_429823.2:n.3415C>T
XR_429823.3:n.3415C>T
XR_429824.2:n.3516C>T
XR_429824.3:n.3516C>T