Canonical Allele Identifier: CA14394907
Community Standard Title: NM_025099.6(CTC1):c.793-112T>A
Gene: CTC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8236454A>T , CM000679.2:g.8236454A>T GRCh38
NC_000017.10:g.8139772A>T , CM000679.1:g.8139772A>T GRCh37
NC_000017.9:g.8080497A>T NCBI36
NG_032148.1:g.16642T>A
NG_032148.2:g.16642T>A

Transcript Alleles

HGVS Amino-acid Change
NM_025099.6:c.793-112T>A MANE Select NP_079375.3:n.793-112T>A
ENST00000651323.1:c.793-112T>A MANE Select ENSP00000498499.1:n.793-112T>A
NM_025099.5:c.793-112T>A NP_079375.3:n.793-112T>A
NR_046431.1:n.747-112T>A
NR_046431.2:n.708-112T>A
ENST00000315684.12:c.793-112T>A ENSP00000313759.8:n.793-112T>A
ENST00000449476.6:c.688-112T>A ENSP00000396018.2:n.688-112T>A
ENST00000449476.7:c.688-112T>A ENSP00000396018.2:n.688-112T>A
ENST00000580299.2:c.793-112T>A ENSP00000462607.2:n.793-112T>A
ENST00000581671.1:n.634-112T>A
ENST00000581671.2:n.634-112T>A
ENST00000581729.2:c.793-112T>A ENSP00000462720.2:n.793-112T>A
ENST00000581967.2:n.815-112T>A
ENST00000583254.2:n.207-112T>A
ENST00000643543.1:c.793-112T>A ENSP00000494323.1:n.793-112T>A
ENST00000699849.1:c.-105-112T>A ENSP00000514647.1:n.-105-112T>A
ENST00000699850.1:n.56-112T>A
ENST00000699851.1:n.815-112T>A
ENST00000699852.1:c.793-112T>A ENSP00000514648.1:n.793-112T>A
ENST00000699853.1:c.793-112T>A ENSP00000514649.1:n.793-112T>A
ENST00000699854.1:n.586-112T>A
ENST00000699855.1:n.815-112T>A
ENST00000699856.1:c.793-112T>A ENSP00000514650.1:n.793-112T>A
ENST00000699857.1:n.801-112T>A
ENST00000699858.1:c.793-112T>A ENSP00000514651.1:n.793-112T>A
ENST00000699859.1:c.793-112T>A ENSP00000514652.1:n.793-112T>A
ENST00000699861.1:n.815-112T>A
ENST00000699862.1:n.680-112T>A
XM_006721577.2:c.793-112T>A XP_006721640.1:n.793-112T>A
XM_006721577.3:c.793-112T>A XP_006721640.1:n.793-112T>A
XM_006721578.2:c.793-112T>A XP_006721641.1:n.793-112T>A
XM_006721578.3:c.793-112T>A XP_006721641.1:n.793-112T>A
XM_006721579.2:c.793-112T>A XP_006721642.1:n.793-112T>A
XM_011524010.1:c.688-112T>A XP_011522312.1:n.688-112T>A
XM_011524010.2:c.688-112T>A XP_011522312.1:n.688-112T>A
XM_011524011.1:c.-109-108T>A XP_011522313.1:n.-109-108T>A
XM_011524011.2:c.-109-108T>A XP_011522313.1:n.-109-108T>A
XR_001752639.1:n.836-112T>A
XR_001752640.1:n.836-112T>A
XR_001752641.1:n.836-112T>A
XR_001752642.1:n.836-112T>A
XR_001752643.1:n.836-112T>A
XR_001752644.1:n.836-112T>A
XR_002958073.1:n.836-112T>A
XR_429823.2:n.836-112T>A
XR_429823.3:n.836-112T>A
XR_429824.2:n.836-112T>A
XR_429824.3:n.836-112T>A
XR_429825.1:n.836-112T>A