Canonical Allele Identifier: CA858138342
Gene: FKTN HGNC NCBI

Linked Data

dbSNP Id: rs1270614334

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.105573757_105573762del , CM000671.2:g.105573757_105573762del GRCh38
NC_000009.11:g.108336038_108336043del , CM000671.1:g.108336038_108336043del GRCh37
NC_000009.10:g.107375859_107375864del NCBI36
NG_008754.1:g.20628_20633del , LRG_434:g.20628_20633del

Transcript Alleles

HGVS Amino-acid Change
ENST00000357998.10:c.-89+11_-89+16del MANE Select ENSP00000350687.6:n.-89+11_-89+16del
ENST00000602661.6:c.-170+11_-170+16del ENSP00000473540.2:n.-170+11_-170+16del
ENST00000674563.1:c.-89+11_-89+16del ENSP00000502153.1:n.-89+11_-89+16del
ENST00000675232.1:c.-89+11_-89+16del ENSP00000502043.1:n.-89+11_-89+16del
ENST00000675443.1:c.-88-1188_-88-1183del ENSP00000502643.1:n.-88-1188_-88-1183del
ENST00000675668.1:c.-224+11_-224+16del ENSP00000502113.1:n.-224+11_-224+16del
ENST00000675695.1:c.-89+11_-89+16del ENSP00000502460.1:n.-89+11_-89+16del
ENST00000675736.1:c.-89+11_-89+16del ENSP00000502809.1:n.-89+11_-89+16del
ENST00000223528.6:c.-88-1188_-88-1183del ENSP00000223528.2:n.-88-1188_-88-1183del
ENST00000448551.6:c.-89+11_-89+16del ENSP00000399140.2:n.-89+11_-89+16del
ENST00000479846.1:n.108+11_108+16del
ENST00000490134.1:n.26-1188_26-1183del
ENST00000602661.5:c.-89+11_-89+16del ENSP00000473540.1:n.-89+11_-89+16del
NM_001079802.1:c.-89+11_-89+16del , LRG_434t1:c.-89+11_-89+16del NP_001073270.1:n.-89+11_-89+16del
NM_001198963.1:c.-89+11_-89+16del NP_001185892.1:n.-89+11_-89+16del
NM_006731.2:c.-88-1188_-88-1183del , LRG_434t2:c.-88-1188_-88-1183del NP_006722.2:n.-88-1188_-88-1183del
XM_006717014.2:c.-88-1188_-88-1183del XP_006717077.1:n.-88-1188_-88-1183del
XM_011518368.1:c.-224+11_-224+16del XP_011516670.1:n.-224+11_-224+16del
XM_011518369.1:c.-89+11_-89+16del XP_011516671.1:n.-89+11_-89+16del
XM_011518370.1:c.-224+11_-224+16del XP_011516672.1:n.-224+11_-224+16del
XM_011518371.1:c.-224+11_-224+16del XP_011516673.1:n.-224+11_-224+16del
XM_011518372.1:c.-224+11_-224+16del XP_011516674.1:n.-224+11_-224+16del
XM_011518373.1:c.-170+11_-170+16del XP_011516675.1:n.-170+11_-170+16del
XM_011518374.1:c.-88-1188_-88-1183del XP_011516676.1:n.-88-1188_-88-1183del
XM_011518376.1:c.-88-1188_-88-1183del XP_011516678.1:n.-88-1188_-88-1183del
XM_011518377.1:c.-224+11_-224+16del XP_011516679.1:n.-224+11_-224+16del
XM_011518378.1:c.-224+11_-224+16del XP_011516680.1:n.-224+11_-224+16del
XM_011518380.1:c.-224+11_-224+16del XP_011516682.1:n.-224+11_-224+16del
XM_011518381.1:c.-345-1188_-345-1183del XP_011516683.1:n.-345-1188_-345-1183del
XM_011518386.1:c.-224+11_-224+16del XP_011516688.1:n.-224+11_-224+16del
XM_011518387.1:c.-224+11_-224+16del XP_011516689.1:n.-224+11_-224+16del
XM_011518388.1:c.-224+11_-224+16del XP_011516690.1:n.-224+11_-224+16del
XM_011518389.1:c.-224+11_-224+16del XP_011516691.1:n.-224+11_-224+16del
XM_011518391.1:c.-224+11_-224+16del XP_011516693.1:n.-224+11_-224+16del
NM_001351496.1:c.-224+11_-224+16del NP_001338425.1:n.-224+11_-224+16del
NM_001351497.1:c.-391+11_-391+16del NP_001338426.1:n.-391+11_-391+16del
NM_001351498.1:c.-88-1188_-88-1183del NP_001338427.1:n.-88-1188_-88-1183del
NM_001351499.1:c.-738+11_-738+16del NP_001338428.1:n.-738+11_-738+16del
NM_001351500.1:c.-603+11_-603+16del NP_001338429.1:n.-603+11_-603+16del
NM_001351501.1:c.-602-1188_-602-1183del NP_001338430.1:n.-602-1188_-602-1183del
NM_001351502.1:c.-684+11_-684+16del NP_001338431.1:n.-684+11_-684+16del
NR_147213.1:n.128+11_128+16del
NR_147214.1:n.37-1188_37-1183del
XM_011518368.2:c.-224+11_-224+16del XP_011516670.1:n.-224+11_-224+16del
XM_011518369.2:c.-89+11_-89+16del XP_011516671.1:n.-89+11_-89+16del
XM_011518370.2:c.-224+11_-224+16del XP_011516672.1:n.-224+11_-224+16del
XM_011518371.2:c.-224+11_-224+16del XP_011516673.1:n.-224+11_-224+16del
XM_011518373.2:c.-170+11_-170+16del XP_011516675.1:n.-170+11_-170+16del
XM_011518374.2:c.-88-1188_-88-1183del XP_011516676.1:n.-88-1188_-88-1183del
XM_011518376.2:c.-88-1188_-88-1183del XP_011516678.1:n.-88-1188_-88-1183del
XM_011518378.2:c.-224+11_-224+16del XP_011516680.1:n.-224+11_-224+16del
XM_011518381.3:c.-345-1188_-345-1183del XP_011516683.1:n.-345-1188_-345-1183del
XM_011518387.2:c.-224+11_-224+16del XP_011516689.1:n.-224+11_-224+16del
XM_011518391.2:c.-224+11_-224+16del XP_011516693.1:n.-224+11_-224+16del
XM_017014462.1:c.-224+11_-224+16del XP_016869951.1:n.-224+11_-224+16del
XM_017014463.1:c.-88-1188_-88-1183del XP_016869952.1:n.-88-1188_-88-1183del
XM_017014464.1:c.-224+11_-224+16del XP_016869953.1:n.-224+11_-224+16del
XM_017014465.1:c.-89+11_-89+16del XP_016869954.1:n.-89+11_-89+16del
XM_017014467.1:c.-89+11_-89+16del XP_016869956.1:n.-89+11_-89+16del
XM_017014468.1:c.-88-1188_-88-1183del XP_016869957.1:n.-88-1188_-88-1183del
XM_017014469.1:c.-224+11_-224+16del XP_016869958.1:n.-224+11_-224+16del
XM_017014470.1:c.-224+11_-224+16del XP_016869959.1:n.-224+11_-224+16del
XM_017014472.2:c.-534+11_-534+16del XP_016869961.1:n.-534+11_-534+16del
XM_017014475.1:c.-88-1188_-88-1183del XP_016869964.1:n.-88-1188_-88-1183del
XR_001746242.2:n.141+11_141+16del
XR_001746243.2:n.141+11_141+16del
XR_001746244.2:n.141+11_141+16del
XR_001746245.1:n.126+11_126+16del
XR_001746248.1:n.1101+11_1101+16del
XR_002956770.1:n.126+11_126+16del
NM_001079802.2:c.-89+11_-89+16del MANE Select NP_001073270.1:n.-89+11_-89+16del
NM_001198963.2:c.-89+11_-89+16del NP_001185892.1:n.-89+11_-89+16del
NM_001351496.2:c.-224+11_-224+16del NP_001338425.1:n.-224+11_-224+16del
NM_001351497.2:c.-391+11_-391+16del NP_001338426.1:n.-391+11_-391+16del
NM_001351498.2:c.-88-1188_-88-1183del NP_001338427.1:n.-88-1188_-88-1183del
NM_001351499.2:c.-738+11_-738+16del NP_001338428.1:n.-738+11_-738+16del
NM_001351500.2:c.-603+11_-603+16del NP_001338429.1:n.-603+11_-603+16del
NM_001351501.2:c.-602-1188_-602-1183del NP_001338430.1:n.-602-1188_-602-1183del
NM_001351502.2:c.-684+11_-684+16del NP_001338431.1:n.-684+11_-684+16del
NR_147213.2:n.127+11_127+16del
NR_147214.2:n.36-1188_36-1183del