Canonical Allele Identifier: CA1870285861
Gene: FKTN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.105636177A= , CM000671.2:g.105636177A= GRCh38
NC_000009.11:g.108398458A= , CM000671.1:g.108398458A= GRCh37
NC_000009.10:g.107438279A= NCBI36
NG_008754.1:g.83048A= , LRG_434:g.83048A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000357998.10:c.*913A= MANE Select ENSP00000350687.6:n.*913A=
ENST00000602661.6:c.*1907A= ENSP00000473540.2:n.*1907A=
ENST00000642177.1:c.*486-496A= ENSP00000495864.1:n.*486-496A=
ENST00000642537.1:c.*1539-496A= ENSP00000495945.1:n.*1539-496A=
ENST00000642952.1:c.1610+1029A= ENSP00000493886.1:n.1610+1029A=
ENST00000644273.1:c.553+1029A=
ENST00000645933.1:c.*1584-496A= ENSP00000495852.1:n.*1584-496A=
ENST00000674563.1:c.*1280A= ENSP00000502153.1:n.*1280A=
ENST00000674633.1:c.1270+1029A= ENSP00000502164.1:n.1270+1029A=
ENST00000675695.1:c.*1280A= ENSP00000502460.1:n.*1280A=
ENST00000675736.1:c.*2079A= ENSP00000502809.1:n.*2079A=
ENST00000676011.1:n.3663A=
ENST00000676310.1:c.1270+1029A= ENSP00000501585.1:n.1270+1029A=
ENST00000223528.6:c.*913A= ENSP00000223528.2:n.*913A=
ENST00000357998.9:c.1270+1029A= ENSP00000350687.5:n.1270+1029A=
ENST00000448551.6:c.1270+1029A= ENSP00000399140.2:n.1270+1029A=
ENST00000457847.1:c.361-496A=
ENST00000602526.1:c.*2337A= ENSP00000473347.1:n.*2337A=
ENST00000602661.5:c.*913A= ENSP00000473540.1:n.*913A=
NM_001079802.1:c.*913A= , LRG_434t1:c.*913A= NP_001073270.1:n.*913A=
NM_001198963.1:c.1270+1029A= NP_001185892.1:n.1270+1029A=
NM_006731.2:c.*913A= , LRG_434t2:c.*913A= NP_006722.2:n.*913A=
XM_006717014.2:c.*1091A= XP_006717077.1:n.*1091A=
NM_001351496.1:c.*913A= NP_001338425.1:n.*913A=
NM_001351497.1:c.*913A= NP_001338426.1:n.*913A=
NM_001351498.1:c.*1091A= NP_001338427.1:n.*1091A=
NM_001351499.1:c.*913A= NP_001338428.1:n.*913A=
NM_001351500.1:c.*913A= NP_001338429.1:n.*913A=
NM_001351501.1:c.*913A= NP_001338430.1:n.*913A=
NM_001351502.1:c.*913A= NP_001338431.1:n.*913A=
NR_147213.1:n.2423A=
NR_147214.1:n.2595A=
XM_011518391.2:c.*1091A= XP_011516693.1:n.*1091A=
XM_017014464.1:c.1270+1029A= XP_016869953.1:n.1270+1029A=
XM_017014465.1:c.1270+1029A= XP_016869954.1:n.1270+1029A=
XM_017014467.1:c.*913A= XP_016869956.1:n.*913A=
XM_017014468.1:c.*913A= XP_016869957.1:n.*913A=
XM_017014469.1:c.1270+1029A= XP_016869958.1:n.1270+1029A=
XM_017014470.1:c.1270+1029A= XP_016869959.1:n.1270+1029A=
XR_001746242.2:n.1837+1029A=
XR_001746244.2:n.1665+1029A=
XR_001746245.1:n.2685A=
XR_001746248.1:n.3778A=
XR_002956770.1:n.2541A=
NM_001079802.2:c.*913A= MANE Select NP_001073270.1:n.*913A=
NM_001198963.2:c.1270+1029A= NP_001185892.1:n.1270+1029A=
NM_001351496.2:c.*913A= NP_001338425.1:n.*913A=
NM_001351497.2:c.*913A= NP_001338426.1:n.*913A=
NM_001351498.2:c.*1091A= NP_001338427.1:n.*1091A=
NM_001351499.2:c.*913A= NP_001338428.1:n.*913A=
NM_001351500.2:c.*913A= NP_001338429.1:n.*913A=
NM_001351501.2:c.*913A= NP_001338430.1:n.*913A=
NM_001351502.2:c.*913A= NP_001338431.1:n.*913A=
NR_147213.2:n.2422A=
NR_147214.2:n.2594A=