Canonical Allele Identifier: CA1870285785
Gene: FKTN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.105636130T= , CM000671.2:g.105636130T= GRCh38
NC_000009.11:g.108398411T= , CM000671.1:g.108398411T= GRCh37
NC_000009.10:g.107438232T= NCBI36
NG_008754.1:g.83001T= , LRG_434:g.83001T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000357998.10:c.*866T= MANE Select ENSP00000350687.6:n.*866T=
ENST00000602661.6:c.*1860T= ENSP00000473540.2:n.*1860T=
ENST00000642177.1:c.*486-543T= ENSP00000495864.1:n.*486-543T=
ENST00000642537.1:c.*1539-543T= ENSP00000495945.1:n.*1539-543T=
ENST00000642952.1:c.1610+982T= ENSP00000493886.1:n.1610+982T=
ENST00000644273.1:c.553+982T=
ENST00000645933.1:c.*1584-543T= ENSP00000495852.1:n.*1584-543T=
ENST00000674563.1:c.*1233T= ENSP00000502153.1:n.*1233T=
ENST00000674633.1:c.1270+982T= ENSP00000502164.1:n.1270+982T=
ENST00000675695.1:c.*1233T= ENSP00000502460.1:n.*1233T=
ENST00000675736.1:c.*2032T= ENSP00000502809.1:n.*2032T=
ENST00000676011.1:n.3616T=
ENST00000676310.1:c.1270+982T= ENSP00000501585.1:n.1270+982T=
ENST00000223528.6:c.*866T= ENSP00000223528.2:n.*866T=
ENST00000357998.9:c.1270+982T= ENSP00000350687.5:n.1270+982T=
ENST00000448551.6:c.1270+982T= ENSP00000399140.2:n.1270+982T=
ENST00000457847.1:c.361-543T=
ENST00000602526.1:c.*2290T= ENSP00000473347.1:n.*2290T=
ENST00000602661.5:c.*866T= ENSP00000473540.1:n.*866T=
NM_001079802.1:c.*866T= , LRG_434t1:c.*866T= NP_001073270.1:n.*866T=
NM_001198963.1:c.1270+982T= NP_001185892.1:n.1270+982T=
NM_006731.2:c.*866T= , LRG_434t2:c.*866T= NP_006722.2:n.*866T=
XM_006717014.2:c.*1044T= XP_006717077.1:n.*1044T=
NM_001351496.1:c.*866T= NP_001338425.1:n.*866T=
NM_001351497.1:c.*866T= NP_001338426.1:n.*866T=
NM_001351498.1:c.*1044T= NP_001338427.1:n.*1044T=
NM_001351499.1:c.*866T= NP_001338428.1:n.*866T=
NM_001351500.1:c.*866T= NP_001338429.1:n.*866T=
NM_001351501.1:c.*866T= NP_001338430.1:n.*866T=
NM_001351502.1:c.*866T= NP_001338431.1:n.*866T=
NR_147213.1:n.2376T=
NR_147214.1:n.2548T=
XM_011518391.2:c.*1044T= XP_011516693.1:n.*1044T=
XM_017014464.1:c.1270+982T= XP_016869953.1:n.1270+982T=
XM_017014465.1:c.1270+982T= XP_016869954.1:n.1270+982T=
XM_017014467.1:c.*866T= XP_016869956.1:n.*866T=
XM_017014468.1:c.*866T= XP_016869957.1:n.*866T=
XM_017014469.1:c.1270+982T= XP_016869958.1:n.1270+982T=
XM_017014470.1:c.1270+982T= XP_016869959.1:n.1270+982T=
XR_001746242.2:n.1837+982T=
XR_001746244.2:n.1665+982T=
XR_001746245.1:n.2638T=
XR_001746248.1:n.3731T=
XR_002956770.1:n.2494T=
NM_001079802.2:c.*866T= MANE Select NP_001073270.1:n.*866T=
NM_001198963.2:c.1270+982T= NP_001185892.1:n.1270+982T=
NM_001351496.2:c.*866T= NP_001338425.1:n.*866T=
NM_001351497.2:c.*866T= NP_001338426.1:n.*866T=
NM_001351498.2:c.*1044T= NP_001338427.1:n.*1044T=
NM_001351499.2:c.*866T= NP_001338428.1:n.*866T=
NM_001351500.2:c.*866T= NP_001338429.1:n.*866T=
NM_001351501.2:c.*866T= NP_001338430.1:n.*866T=
NM_001351502.2:c.*866T= NP_001338431.1:n.*866T=
NR_147213.2:n.2375T=
NR_147214.2:n.2547T=