Canonical Allele Identifier: CA497958783
Gene: CTC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.8135077T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8231759T>A , CM000679.2:g.8231759T>A GRCh38
NC_000017.10:g.8135077T>A , CM000679.1:g.8135077T>A GRCh37
NC_000017.9:g.8075802T>A NCBI36
NG_032148.1:g.21337A>T
NG_032148.2:g.21337A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000580299.2:c.2442A>T ENSP00000462607.2:p.Gly814=
ENST00000581729.2:c.2442A>T ENSP00000462720.2:p.Gly814=
ENST00000581967.2:n.2894A>T
ENST00000583254.2:n.3235A>T
ENST00000699849.1:c.1545A>T ENSP00000514647.1:p.Gly515=
ENST00000699850.1:n.1705A>T
ENST00000699851.1:n.2464A>T
ENST00000699852.1:c.*1118A>T ENSP00000514648.1:n.*1118A>T
ENST00000699853.1:c.2442A>T ENSP00000514649.1:p.Gly814=
ENST00000699854.1:n.2235A>T
ENST00000699855.1:n.2894A>T
ENST00000699856.1:c.2442A>T ENSP00000514650.1:p.Gly814=
ENST00000699857.1:n.2450A>T
ENST00000699858.1:c.*1055A>T ENSP00000514651.1:n.*1055A>T
ENST00000699859.1:c.2313A>T ENSP00000514652.1:p.Gly771=
ENST00000699860.1:n.548A>T
ENST00000699861.1:n.2464A>T
ENST00000699862.1:n.3402A>T
ENST00000449476.7:c.2337A>T ENSP00000396018.2:p.Gly779=
ENST00000581671.2:n.2431A>T
ENST00000643543.1:c.*1149A>T ENSP00000494323.1:n.*1149A>T
ENST00000651323.1:c.2442A>T MANE Select ENSP00000498499.1:p.Gly814=
ENST00000315684.12:c.2442A>T ENSP00000313759.8:p.Gly814=
ENST00000449476.6:c.2337A>T ENSP00000396018.2:p.Gly779=
ENST00000578240.1:n.670A>T
ENST00000578537.1:c.338A>T
NM_025099.5:c.2442A>T NP_079375.3:p.Gly814=
NR_046431.1:n.2396A>T
XM_006721577.2:c.2313A>T XP_006721640.1:p.Gly771=
XM_006721578.2:c.2442A>T XP_006721641.1:p.Gly814=
XM_006721579.2:c.2442A>T XP_006721642.1:p.Gly814=
XM_011524010.1:c.2337A>T XP_011522312.1:p.Gly779=
XM_011524011.1:c.1545A>T XP_011522313.1:p.Gly515=
XR_429823.2:n.2485A>T
XR_429824.2:n.2485A>T
XR_429825.1:n.2485A>T
NM_025099.6:c.2442A>T MANE Select NP_079375.3:p.Gly814=
XM_006721577.3:c.2313A>T XP_006721640.1:p.Gly771=
XM_006721578.3:c.2442A>T XP_006721641.1:p.Gly814=
XM_011524010.2:c.2337A>T XP_011522312.1:p.Gly779=
XM_011524011.2:c.1545A>T XP_011522313.1:p.Gly515=
XR_001752639.1:n.2356A>T
XR_001752640.1:n.2485A>T
XR_001752641.1:n.2485A>T
XR_001752642.1:n.2485A>T
XR_001752643.1:n.2915A>T
XR_002958073.1:n.2485A>T
XR_429823.3:n.2485A>T
XR_429824.3:n.2485A>T
NR_046431.2:n.2357A>T