Canonical Allele Identifier: CA397976514
Gene: CTC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8231734C>T , CM000679.2:g.8231734C>T GRCh38
NC_000017.10:g.8135052C>T , CM000679.1:g.8135052C>T GRCh37
NC_000017.9:g.8075777C>T NCBI36
NG_032148.1:g.21362G>A
NG_032148.2:g.21362G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000580299.2:c.2467G>A ENSP00000462607.2:p.Gly823Ser
ENST00000581729.2:c.2467G>A ENSP00000462720.2:p.Gly823Ser
ENST00000581967.2:n.2919G>A
ENST00000583254.2:n.3260G>A
ENST00000699849.1:c.1570G>A ENSP00000514647.1:p.Gly524Ser
ENST00000699850.1:n.1730G>A
ENST00000699851.1:n.2489G>A
ENST00000699852.1:c.*1143G>A ENSP00000514648.1:n.*1143G>A
ENST00000699853.1:c.2467G>A ENSP00000514649.1:p.Gly823Ser
ENST00000699854.1:n.2260G>A
ENST00000699855.1:n.2919G>A
ENST00000699856.1:c.2467G>A ENSP00000514650.1:p.Gly823Ser
ENST00000699857.1:n.2475G>A
ENST00000699858.1:c.*1080G>A ENSP00000514651.1:n.*1080G>A
ENST00000699859.1:c.2338G>A ENSP00000514652.1:p.Gly780Ser
ENST00000699860.1:n.573G>A
ENST00000699861.1:n.2489G>A
ENST00000699862.1:n.3427G>A
ENST00000449476.7:c.2362G>A ENSP00000396018.2:p.Gly788Ser
ENST00000581671.2:n.2456G>A
ENST00000643543.1:c.*1174G>A ENSP00000494323.1:n.*1174G>A
ENST00000651323.1:c.2467G>A MANE Select ENSP00000498499.1:p.Gly823Ser
ENST00000315684.12:c.2467G>A ENSP00000313759.8:p.Gly823Ser
ENST00000449476.6:c.2362G>A ENSP00000396018.2:p.Gly788Ser
ENST00000578240.1:n.695G>A
ENST00000578537.1:c.363G>A
NM_025099.5:c.2467G>A NP_079375.3:p.Gly823Ser
NR_046431.1:n.2421G>A
XM_006721577.2:c.2338G>A XP_006721640.1:p.Gly780Ser
XM_006721578.2:c.2467G>A XP_006721641.1:p.Gly823Ser
XM_006721579.2:c.2467G>A XP_006721642.1:p.Gly823Ser
XM_011524010.1:c.2362G>A XP_011522312.1:p.Gly788Ser
XM_011524011.1:c.1570G>A XP_011522313.1:p.Gly524Ser
XR_429823.2:n.2510G>A
XR_429824.2:n.2510G>A
XR_429825.1:n.2510G>A
NM_025099.6:c.2467G>A MANE Select NP_079375.3:p.Gly823Ser
XM_006721577.3:c.2338G>A XP_006721640.1:p.Gly780Ser
XM_006721578.3:c.2467G>A XP_006721641.1:p.Gly823Ser
XM_011524010.2:c.2362G>A XP_011522312.1:p.Gly788Ser
XM_011524011.2:c.1570G>A XP_011522313.1:p.Gly524Ser
XR_001752639.1:n.2381G>A
XR_001752640.1:n.2510G>A
XR_001752641.1:n.2510G>A
XR_001752642.1:n.2510G>A
XR_001752643.1:n.2940G>A
XR_002958073.1:n.2510G>A
XR_429823.3:n.2510G>A
XR_429824.3:n.2510G>A
NR_046431.2:n.2382G>A