Canonical Allele Identifier: CA2246180986
Gene: CTC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8237407G= , CM000679.2:g.8237407G= GRCh38
NC_000017.10:g.8140725G= , CM000679.1:g.8140725G= GRCh37
NC_000017.9:g.8081450G= NCBI36
NG_032148.1:g.15689C=
NG_032148.2:g.15689C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000580299.2:c.760C= ENSP00000462607.2:p.Pro254=
ENST00000581729.2:c.760C= ENSP00000462720.2:p.Pro254=
ENST00000581967.2:n.782C=
ENST00000583254.2:n.174C=
ENST00000699849.1:c.-138C= ENSP00000514647.1:n.-138C=
ENST00000699850.1:n.56-1065C=
ENST00000699851.1:n.782C=
ENST00000699852.1:c.760C= ENSP00000514648.1:p.Pro254=
ENST00000699853.1:c.760C= ENSP00000514649.1:p.Pro254=
ENST00000699854.1:n.553C=
ENST00000699855.1:n.782C=
ENST00000699856.1:c.760C= ENSP00000514650.1:p.Pro254=
ENST00000699857.1:n.768C=
ENST00000699858.1:c.760C= ENSP00000514651.1:p.Pro254=
ENST00000699859.1:c.760C= ENSP00000514652.1:p.Pro254=
ENST00000699861.1:n.782C=
ENST00000699862.1:n.647C=
ENST00000449476.7:c.655C= ENSP00000396018.2:p.Pro219=
ENST00000581671.2:n.601C=
ENST00000643543.1:c.760C= ENSP00000494323.1:p.Pro254=
ENST00000651323.1:c.760C= MANE Select ENSP00000498499.1:p.Pro254=
ENST00000315684.12:c.760C= ENSP00000313759.8:p.Pro254=
ENST00000449476.6:c.655C= ENSP00000396018.2:p.Pro219=
ENST00000581671.1:n.601C=
NM_025099.5:c.760C= NP_079375.3:p.Pro254=
NR_046431.1:n.714C=
XM_006721577.2:c.760C= XP_006721640.1:p.Pro254=
XM_006721578.2:c.760C= XP_006721641.1:p.Pro254=
XM_006721579.2:c.760C= XP_006721642.1:p.Pro254=
XM_011524010.1:c.655C= XP_011522312.1:p.Pro219=
XM_011524011.1:c.-142C= XP_011522313.1:n.-142C=
XR_429823.2:n.803C=
XR_429824.2:n.803C=
XR_429825.1:n.803C=
NM_025099.6:c.760C= MANE Select NP_079375.3:p.Pro254=
XM_006721577.3:c.760C= XP_006721640.1:p.Pro254=
XM_006721578.3:c.760C= XP_006721641.1:p.Pro254=
XM_011524010.2:c.655C= XP_011522312.1:p.Pro219=
XM_011524011.2:c.-142C= XP_011522313.1:n.-142C=
XR_001752639.1:n.803C=
XR_001752640.1:n.803C=
XR_001752641.1:n.803C=
XR_001752642.1:n.803C=
XR_001752643.1:n.803C=
XR_001752644.1:n.803C=
XR_002958073.1:n.803C=
XR_429823.3:n.803C=
XR_429824.3:n.803C=
NR_046431.2:n.675C=