Canonical Allele Identifier: CA8372560
Gene: CTC1 HGNC NCBI

Linked Data

dbSNP Id: rs767351989

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8237363_8237380del , CM000679.2:g.8237363_8237380del GRCh38
NC_000017.10:g.8140681_8140698del , CM000679.1:g.8140681_8140698del GRCh37
NC_000017.9:g.8081406_8081423del NCBI36
NG_032148.1:g.15718_15735del
NG_032148.2:g.15718_15735del

Transcript Alleles

HGVS Amino-acid Change
ENST00000580299.2:c.789_792+14del
ENST00000581729.2:c.789_792+14del
ENST00000581967.2:n.811_814+14del
ENST00000583254.2:n.203_206+14del
ENST00000699849.1:c.-109_-106+14del
ENST00000699850.1:n.56-1036_56-1019del
ENST00000699851.1:n.811_814+14del
ENST00000699852.1:c.789_792+14del
ENST00000699853.1:c.789_792+14del
ENST00000699854.1:n.582_585+14del
ENST00000699855.1:n.811_814+14del
ENST00000699856.1:c.789_792+14del
ENST00000699857.1:n.797_800+14del
ENST00000699858.1:c.789_792+14del
ENST00000699859.1:c.789_792+14del
ENST00000699861.1:n.811_814+14del
ENST00000699862.1:n.676_679+14del
ENST00000449476.7:c.684_687+14del
ENST00000581671.2:n.630_633+14del
ENST00000643543.1:c.789_792+14del
ENST00000651323.1:c.789_792+14del
ENST00000315684.12:c.789_792+14del
ENST00000449476.6:c.684_687+14del
ENST00000581671.1:n.630_633+14del
NM_025099.5:c.789_792+14del
NR_046431.1:n.743_746+14del
XM_006721577.2:c.789_792+14del
XM_006721578.2:c.789_792+14del
XM_006721579.2:c.789_792+14del
XM_011524010.1:c.684_687+14del
XM_011524011.1:c.-113_-110+14del
XR_429823.2:n.832_835+14del
XR_429824.2:n.832_835+14del
XR_429825.1:n.832_835+14del
NM_025099.6:c.789_792+14del
XM_006721577.3:c.789_792+14del
XM_006721578.3:c.789_792+14del
XM_011524010.2:c.684_687+14del
XM_011524011.2:c.-113_-110+14del
XR_001752639.1:n.832_835+14del
XR_001752640.1:n.832_835+14del
XR_001752641.1:n.832_835+14del
XR_001752642.1:n.832_835+14del
XR_001752643.1:n.832_835+14del
XR_001752644.1:n.832_835+14del
XR_002958073.1:n.832_835+14del
XR_429823.3:n.832_835+14del
XR_429824.3:n.832_835+14del
NR_046431.2:n.704_707+14del