Canonical Allele Identifier: CA1870286847
Gene: FKTN HGNC NCBI

Linked Data

dbSNP Id: rs1834055202

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.105636596_105636597insGTATCTGAA , CM000671.2:g.105636596_105636597insGTATCTGAA GRCh38
NC_000009.11:g.108398877_108398878insGTATCTGAA , CM000671.1:g.108398877_108398878insGTATCTGAA GRCh37
NC_000009.10:g.107438698_107438699insGTATCTGAA NCBI36
NG_008754.1:g.83467_83468insGTATCTGAA , LRG_434:g.83467_83468insGTATCTGAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000357998.10:c.*1332_*1333insGTATCTGAA MANE Select ENSP00000350687.6:n.*1332_*1333insGTATCTGAA
ENST00000642177.1:c.*486-77_*486-76insGTATCTGAA ENSP00000495864.1:n.*486-77_*486-76insGTATCTGAA
ENST00000642537.1:c.*1539-77_*1539-76insGTATCTGAA ENSP00000495945.1:n.*1539-77_*1539-76insGTATCTGAA
ENST00000642952.1:c.1610+1448_1610+1449insGTATCTGAA ENSP00000493886.1:n.1610+1448_1610+1449insGTATCTGAA
ENST00000644273.1:c.553+1448_553+1449insGTATCTGAA
ENST00000645933.1:c.*1584-77_*1584-76insGTATCTGAA ENSP00000495852.1:n.*1584-77_*1584-76insGTATCTGAA
ENST00000674563.1:c.*1699_*1700insGTATCTGAA ENSP00000502153.1:n.*1699_*1700insGTATCTGAA
ENST00000674633.1:c.1270+1448_1270+1449insGTATCTGAA ENSP00000502164.1:n.1270+1448_1270+1449insGTATCTGAA
ENST00000675695.1:c.*1699_*1700insGTATCTGAA ENSP00000502460.1:n.*1699_*1700insGTATCTGAA
ENST00000675736.1:c.*2498_*2499insGTATCTGAA ENSP00000502809.1:n.*2498_*2499insGTATCTGAA
ENST00000676011.1:n.4082_4083insGTATCTGAA
ENST00000676310.1:c.1270+1448_1270+1449insGTATCTGAA ENSP00000501585.1:n.1270+1448_1270+1449insGTATCTGAA
ENST00000223528.6:c.*1332_*1333insGTATCTGAA ENSP00000223528.2:n.*1332_*1333insGTATCTGAA
ENST00000357998.9:c.1270+1448_1270+1449insGTATCTGAA ENSP00000350687.5:n.1270+1448_1270+1449insGTATCTGAA
ENST00000448551.6:c.1270+1448_1270+1449insGTATCTGAA ENSP00000399140.2:n.1270+1448_1270+1449insGTATCTGAA
ENST00000457847.1:c.361-77_361-76insGTATCTGAA
ENST00000602526.1:c.*2756_*2757insGTATCTGAA ENSP00000473347.1:n.*2756_*2757insGTATCTGAA
NM_001079802.1:c.*1332_*1333insGTATCTGAA , LRG_434t1:c.*1332_*1333insGTATCTGAA NP_001073270.1:n.*1332_*1333insGTATCTGAA
NM_001198963.1:c.1270+1448_1270+1449insGTATCTGAA NP_001185892.1:n.1270+1448_1270+1449insGTATCTGAA
NM_006731.2:c.*1332_*1333insGTATCTGAA , LRG_434t2:c.*1332_*1333insGTATCTGAA NP_006722.2:n.*1332_*1333insGTATCTGAA
XM_006717014.2:c.*1510_*1511insGTATCTGAA XP_006717077.1:n.*1510_*1511insGTATCTGAA
NM_001351496.1:c.*1332_*1333insGTATCTGAA NP_001338425.1:n.*1332_*1333insGTATCTGAA
NM_001351497.1:c.*1332_*1333insGTATCTGAA NP_001338426.1:n.*1332_*1333insGTATCTGAA
NM_001351498.1:c.*1510_*1511insGTATCTGAA NP_001338427.1:n.*1510_*1511insGTATCTGAA
NM_001351499.1:c.*1332_*1333insGTATCTGAA NP_001338428.1:n.*1332_*1333insGTATCTGAA
NM_001351500.1:c.*1332_*1333insGTATCTGAA NP_001338429.1:n.*1332_*1333insGTATCTGAA
NM_001351501.1:c.*1332_*1333insGTATCTGAA NP_001338430.1:n.*1332_*1333insGTATCTGAA
NM_001351502.1:c.*1332_*1333insGTATCTGAA NP_001338431.1:n.*1332_*1333insGTATCTGAA
NR_147213.1:n.2842_2843insGTATCTGAA
NR_147214.1:n.3014_3015insGTATCTGAA
XM_011518391.2:c.*1510_*1511insGTATCTGAA XP_011516693.1:n.*1510_*1511insGTATCTGAA
XM_017014464.1:c.1270+1448_1270+1449insGTATCTGAA XP_016869953.1:n.1270+1448_1270+1449insGTATCTGAA
XM_017014465.1:c.1270+1448_1270+1449insGTATCTGAA XP_016869954.1:n.1270+1448_1270+1449insGTATCTGAA
XM_017014467.1:c.*1332_*1333insGTATCTGAA XP_016869956.1:n.*1332_*1333insGTATCTGAA
XM_017014468.1:c.*1332_*1333insGTATCTGAA XP_016869957.1:n.*1332_*1333insGTATCTGAA
XM_017014469.1:c.1270+1448_1270+1449insGTATCTGAA XP_016869958.1:n.1270+1448_1270+1449insGTATCTGAA
XM_017014470.1:c.1270+1448_1270+1449insGTATCTGAA XP_016869959.1:n.1270+1448_1270+1449insGTATCTGAA
XR_001746242.2:n.1837+1448_1837+1449insGTATCTGAA
XR_001746244.2:n.1665+1448_1665+1449insGTATCTGAA
XR_001746245.1:n.3104_3105insGTATCTGAA
XR_001746248.1:n.4197_4198insGTATCTGAA
XR_002956770.1:n.2960_2961insGTATCTGAA
NM_001079802.2:c.*1332_*1333insGTATCTGAA MANE Select NP_001073270.1:n.*1332_*1333insGTATCTGAA
NM_001198963.2:c.1270+1448_1270+1449insGTATCTGAA NP_001185892.1:n.1270+1448_1270+1449insGTATCTGAA
NM_001351496.2:c.*1332_*1333insGTATCTGAA NP_001338425.1:n.*1332_*1333insGTATCTGAA
NM_001351497.2:c.*1332_*1333insGTATCTGAA NP_001338426.1:n.*1332_*1333insGTATCTGAA
NM_001351498.2:c.*1510_*1511insGTATCTGAA NP_001338427.1:n.*1510_*1511insGTATCTGAA
NM_001351499.2:c.*1332_*1333insGTATCTGAA NP_001338428.1:n.*1332_*1333insGTATCTGAA
NM_001351500.2:c.*1332_*1333insGTATCTGAA NP_001338429.1:n.*1332_*1333insGTATCTGAA
NM_001351501.2:c.*1332_*1333insGTATCTGAA NP_001338430.1:n.*1332_*1333insGTATCTGAA
NM_001351502.2:c.*1332_*1333insGTATCTGAA NP_001338431.1:n.*1332_*1333insGTATCTGAA
NR_147213.2:n.2841_2842insGTATCTGAA
NR_147214.2:n.3013_3014insGTATCTGAA