Canonical Allele Identifier: CA2246187403
Gene: CTC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8229943G= , CM000679.2:g.8229943G= GRCh38
NC_000017.10:g.8133261G= , CM000679.1:g.8133261G= GRCh37
NC_000017.9:g.8073986G= NCBI36
NG_032148.1:g.23153C=
NG_032148.2:g.23153C=

Transcript Alleles

HGVS Amino-acid Change
NM_025099.6:c.2959C= MANE Select NP_079375.3:p.Arg987=
ENST00000651323.1:c.2959C= MANE Select ENSP00000498499.1:p.Arg987=
NM_025099.5:c.2959C= NP_079375.3:p.Arg987=
NR_046431.1:n.2913C=
NR_046431.2:n.2874C=
ENST00000315684.12:c.2959C= ENSP00000313759.8:p.Arg987=
ENST00000449476.6:c.2854C= ENSP00000396018.2:p.Arg952=
ENST00000449476.7:c.2854C= ENSP00000396018.2:p.Arg952=
ENST00000578240.1:n.1512C=
ENST00000578441.5:n.337-21C=
ENST00000578537.1:c.636-21C=
ENST00000580299.1:c.130C= ENSP00000462607.1:p.Arg44=
ENST00000580299.2:c.2959C= ENSP00000462607.2:p.Arg987=
ENST00000581671.2:n.2948C=
ENST00000581729.2:c.2959C= ENSP00000462720.2:p.Arg987=
ENST00000581967.2:n.3411C=
ENST00000583254.2:n.4957C=
ENST00000643543.1:c.*1666C= ENSP00000494323.1:n.*1666C=
ENST00000699849.1:c.2062C= ENSP00000514647.1:p.Arg688=
ENST00000699850.1:n.2547C=
ENST00000699851.1:n.3306C=
ENST00000699852.1:c.*1537C= ENSP00000514648.1:n.*1537C=
ENST00000699853.1:c.2959C= ENSP00000514649.1:p.Arg987=
ENST00000699854.1:n.3077C=
ENST00000699855.1:n.3736C=
ENST00000699856.1:c.2934-21C= ENSP00000514650.1:n.2934-21C=
ENST00000699857.1:n.3194C=
ENST00000699858.1:c.*1897C= ENSP00000514651.1:n.*1897C=
ENST00000699859.1:c.2830C= ENSP00000514652.1:p.Arg944=
ENST00000699860.1:n.1196C=
ENST00000699861.1:n.2981C=
ENST00000699862.1:n.4244C=
XM_006721577.2:c.2830C= XP_006721640.1:p.Arg944=
XM_006721577.3:c.2830C= XP_006721640.1:p.Arg944=
XM_006721578.2:c.2959C= XP_006721641.1:p.Arg987=
XM_006721578.3:c.2959C= XP_006721641.1:p.Arg987=
XM_006721579.2:c.2934-21C= XP_006721642.1:n.2934-21C=
XM_011524010.1:c.2854C= XP_011522312.1:p.Arg952=
XM_011524010.2:c.2854C= XP_011522312.1:p.Arg952=
XM_011524011.1:c.2062C= XP_011522313.1:p.Arg688=
XM_011524011.2:c.2062C= XP_011522313.1:p.Arg688=
XR_001752639.1:n.2873C=
XR_001752640.1:n.2977-21C=
XR_001752641.1:n.2977-21C=
XR_001752642.1:n.2808C=
XR_001752643.1:n.3432C=
XR_002958073.1:n.2808C=
XR_429823.2:n.3002C=
XR_429823.3:n.3002C=
XR_429824.2:n.3002C=
XR_429824.3:n.3002C=
XR_429825.1:n.2808C=