Canonical Allele Identifier: CA2580079307
Gene: FKTN HGNC NCBI

Linked Data

ClinVar Variation Id: 2186733
ClinVar RCV Id: RCV002606862

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.105604215del , CM000671.2:g.105604215del GRCh38
NC_000009.11:g.108366496del , CM000671.1:g.108366496del GRCh37
NC_000009.10:g.107406317del NCBI36
NG_008754.1:g.51086del , LRG_434:g.51086del

Transcript Alleles

HGVS Amino-acid change
ENST00000357998.10:c.370del
ENST00000374705.5:c.381del
ENST00000602661.6:c.488del
ENST00000642177.1:c.370del
ENST00000642537.1:c.*232del
ENST00000642644.1:c.*493del
ENST00000642952.1:c.395del
ENST00000645933.1:c.*368del
ENST00000674563.1:c.370del
ENST00000674633.1:c.370del
ENST00000675232.1:c.*505del
ENST00000675443.1:c.488del
ENST00000675668.1:c.370del
ENST00000675695.1:c.370del
ENST00000675736.1:c.488del
ENST00000676011.1:n.1537del
ENST00000676192.1:c.*290del
ENST00000676310.1:c.370del
ENST00000676371.1:c.*177del
ENST00000223528.6:c.370del
ENST00000357998.9:c.370del
ENST00000374705.4:c.301del
ENST00000448551.6:c.370del
ENST00000602526.1:c.*408del
ENST00000602661.5:c.370del
NM_001079802.1:c.370del , LRG_434t1:c.370del
NM_001198963.1:c.370del
NM_006731.2:c.370del , LRG_434t2:c.370del
XM_006717014.2:c.370del
XM_011518368.1:c.370del
XM_011518369.1:c.370del
XM_011518370.1:c.370del
XM_011518371.1:c.370del
XM_011518372.1:c.370del
XM_011518373.1:c.370del
XM_011518374.1:c.370del
XM_011518375.1:c.370del
XM_011518376.1:c.370del
XM_011518377.1:c.370del
XM_011518378.1:c.370del
XM_011518379.1:c.301del
XM_011518380.1:c.370del
XM_011518381.1:c.184del
XM_011518382.1:c.184del
XM_011518383.1:c.184del
XM_011518384.1:c.184del
XM_011518385.1:c.184del
XM_011518386.1:c.370del
XM_011518387.1:c.370del
XM_011518388.1:c.370del
XM_011518389.1:c.370del
XM_011518390.1:c.-27del
XM_011518391.1:c.370del
NM_001351496.1:c.370del
NM_001351497.1:c.301del
NM_001351498.1:c.370del
NM_001351499.1:c.-27del
NM_001351500.1:c.-27del
NM_001351501.1:c.-27del
NM_001351502.1:c.-27del
NR_147213.1:n.586del
NR_147214.1:n.494del
XM_011518368.2:c.370del
XM_011518369.2:c.370del
XM_011518370.2:c.370del
XM_011518371.2:c.370del
XM_011518373.2:c.370del
XM_011518374.2:c.370del
XM_011518375.2:c.370del
XM_011518376.2:c.370del
XM_011518378.2:c.370del
XM_011518379.2:c.301del
XM_011518381.3:c.184del
XM_011518387.2:c.370del
XM_011518390.2:c.-27del
XM_011518391.2:c.370del
XM_017014462.1:c.370del
XM_017014463.1:c.370del
XM_017014464.1:c.370del
XM_017014465.1:c.370del
XM_017014467.1:c.370del
XM_017014468.1:c.370del
XM_017014469.1:c.370del
XM_017014470.1:c.370del
XM_017014472.2:c.184del
XM_017014473.2:c.184del
XM_017014475.1:c.370del
XR_001746242.2:n.734del
XR_001746243.2:n.734del
XR_001746244.2:n.734del
XR_001746245.1:n.584del
XR_001746248.1:n.1677del
XR_002956770.1:n.584del
NM_001079802.2:c.370del
NM_001198963.2:c.370del
NM_001351496.2:c.370del
NM_001351497.2:c.301del
NM_001351498.2:c.370del
NM_001351499.2:c.-27del
NM_001351500.2:c.-27del
NM_001351501.2:c.-27del
NM_001351502.2:c.-27del
NR_147213.2:n.585del
NR_147214.2:n.493del