Canonical Allele Identifier: CA2579409416
Gene: FKTN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.105636120_105636125del , CM000671.2:g.105636120_105636125del GRCh38
NC_000009.11:g.108398401_108398406del , CM000671.1:g.108398401_108398406del GRCh37
NC_000009.10:g.107438222_107438227del NCBI36
NG_008754.1:g.82991_82996del , LRG_434:g.82991_82996del

Transcript Alleles

HGVS Amino-acid Change
ENST00000357998.10:c.*856_*861del MANE Select ENSP00000350687.6:n.*856_*861del
ENST00000602661.6:c.*1850_*1855del ENSP00000473540.2:n.*1850_*1855del
ENST00000642177.1:c.*486-553_*486-548del ENSP00000495864.1:n.*486-553_*486-548del
ENST00000642537.1:c.*1539-553_*1539-548del ENSP00000495945.1:n.*1539-553_*1539-548del
ENST00000642952.1:c.1610+972_1610+977del ENSP00000493886.1:n.1610+972_1610+977del
ENST00000644273.1:c.553+972_553+977del
ENST00000645933.1:c.*1584-553_*1584-548del ENSP00000495852.1:n.*1584-553_*1584-548del
ENST00000674563.1:c.*1223_*1228del ENSP00000502153.1:n.*1223_*1228del
ENST00000674633.1:c.1270+972_1270+977del ENSP00000502164.1:n.1270+972_1270+977del
ENST00000675695.1:c.*1223_*1228del ENSP00000502460.1:n.*1223_*1228del
ENST00000675736.1:c.*2022_*2027del ENSP00000502809.1:n.*2022_*2027del
ENST00000676011.1:n.3606_3611del
ENST00000676310.1:c.1270+972_1270+977del ENSP00000501585.1:n.1270+972_1270+977del
ENST00000223528.6:c.*856_*861del ENSP00000223528.2:n.*856_*861del
ENST00000357998.9:c.1270+972_1270+977del ENSP00000350687.5:n.1270+972_1270+977del
ENST00000448551.6:c.1270+972_1270+977del ENSP00000399140.2:n.1270+972_1270+977del
ENST00000457847.1:c.361-553_361-548del
ENST00000602526.1:c.*2280_*2285del ENSP00000473347.1:n.*2280_*2285del
ENST00000602661.5:c.*856_*861del ENSP00000473540.1:n.*856_*861del
NM_001079802.1:c.*856_*861del , LRG_434t1:c.*856_*861del NP_001073270.1:n.*856_*861del
NM_001198963.1:c.1270+972_1270+977del NP_001185892.1:n.1270+972_1270+977del
NM_006731.2:c.*856_*861del , LRG_434t2:c.*856_*861del NP_006722.2:n.*856_*861del
XM_006717014.2:c.*1034_*1039del XP_006717077.1:n.*1034_*1039del
NM_001351496.1:c.*856_*861del NP_001338425.1:n.*856_*861del
NM_001351497.1:c.*856_*861del NP_001338426.1:n.*856_*861del
NM_001351498.1:c.*1034_*1039del NP_001338427.1:n.*1034_*1039del
NM_001351499.1:c.*856_*861del NP_001338428.1:n.*856_*861del
NM_001351500.1:c.*856_*861del NP_001338429.1:n.*856_*861del
NM_001351501.1:c.*856_*861del NP_001338430.1:n.*856_*861del
NM_001351502.1:c.*856_*861del NP_001338431.1:n.*856_*861del
NR_147213.1:n.2366_2371del
NR_147214.1:n.2538_2543del
XM_011518391.2:c.*1034_*1039del XP_011516693.1:n.*1034_*1039del
XM_017014464.1:c.1270+972_1270+977del XP_016869953.1:n.1270+972_1270+977del
XM_017014465.1:c.1270+972_1270+977del XP_016869954.1:n.1270+972_1270+977del
XM_017014467.1:c.*856_*861del XP_016869956.1:n.*856_*861del
XM_017014468.1:c.*856_*861del XP_016869957.1:n.*856_*861del
XM_017014469.1:c.1270+972_1270+977del XP_016869958.1:n.1270+972_1270+977del
XM_017014470.1:c.1270+972_1270+977del XP_016869959.1:n.1270+972_1270+977del
XR_001746242.2:n.1837+972_1837+977del
XR_001746244.2:n.1665+972_1665+977del
XR_001746245.1:n.2628_2633del
XR_001746248.1:n.3721_3726del
XR_002956770.1:n.2484_2489del
NM_001079802.2:c.*856_*861del MANE Select NP_001073270.1:n.*856_*861del
NM_001198963.2:c.1270+972_1270+977del NP_001185892.1:n.1270+972_1270+977del
NM_001351496.2:c.*856_*861del NP_001338425.1:n.*856_*861del
NM_001351497.2:c.*856_*861del NP_001338426.1:n.*856_*861del
NM_001351498.2:c.*1034_*1039del NP_001338427.1:n.*1034_*1039del
NM_001351499.2:c.*856_*861del NP_001338428.1:n.*856_*861del
NM_001351500.2:c.*856_*861del NP_001338429.1:n.*856_*861del
NM_001351501.2:c.*856_*861del NP_001338430.1:n.*856_*861del
NM_001351502.2:c.*856_*861del NP_001338431.1:n.*856_*861del
NR_147213.2:n.2365_2370del
NR_147214.2:n.2537_2542del