Canonical Allele Identifier: CA2579409441

Gene: FKTN

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.105636585_105636602del , CM000671.2:g.105636585_105636602del	GRCh38
NC_000009.11:g.108398866_108398883del , CM000671.1:g.108398866_108398883del	GRCh37
NC_000009.10:g.107438687_107438704del	NCBI36
NG_008754.1:g.83456_83473del , LRG_434:g.83456_83473del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357998.10:c.*1321_*1338del MANE Select	ENSP00000350687.6:n.*1321_*1338del
ENST00000642177.1:c.*486-88_*486-71del	ENSP00000495864.1:n.*486-88_*486-71del
ENST00000642537.1:c.*1539-88_*1539-71del	ENSP00000495945.1:n.*1539-88_*1539-71del
ENST00000642952.1:c.1610+1437_1610+1454del	ENSP00000493886.1:n.1610+1437_1610+1454del
ENST00000644273.1:c.553+1437_553+1454del
ENST00000645933.1:c.*1584-88_*1584-71del	ENSP00000495852.1:n.*1584-88_*1584-71del
ENST00000674563.1:c.*1688_*1705del	ENSP00000502153.1:n.*1688_*1705del
ENST00000674633.1:c.1270+1437_1270+1454del	ENSP00000502164.1:n.1270+1437_1270+1454del
ENST00000675695.1:c.*1688_*1705del	ENSP00000502460.1:n.*1688_*1705del
ENST00000675736.1:c.*2487_*2504del	ENSP00000502809.1:n.*2487_*2504del
ENST00000676011.1:n.4071_4088del
ENST00000676310.1:c.1270+1437_1270+1454del	ENSP00000501585.1:n.1270+1437_1270+1454del
ENST00000223528.6:c.*1321_*1338del	ENSP00000223528.2:n.*1321_*1338del
ENST00000357998.9:c.1270+1437_1270+1454del	ENSP00000350687.5:n.1270+1437_1270+1454del
ENST00000448551.6:c.1270+1437_1270+1454del	ENSP00000399140.2:n.1270+1437_1270+1454del
ENST00000457847.1:c.361-88_361-71del
ENST00000602526.1:c.*2745_*2762del	ENSP00000473347.1:n.*2745_*2762del
NM_001079802.1:c.*1321_*1338del , LRG_434t1:c.*1321_*1338del	NP_001073270.1:n.*1321_*1338del
NM_001198963.1:c.1270+1437_1270+1454del	NP_001185892.1:n.1270+1437_1270+1454del
NM_006731.2:c.*1321_*1338del , LRG_434t2:c.*1321_*1338del	NP_006722.2:n.*1321_*1338del
XM_006717014.2:c.*1499_*1516del	XP_006717077.1:n.*1499_*1516del
NM_001351496.1:c.*1321_*1338del	NP_001338425.1:n.*1321_*1338del
NM_001351497.1:c.*1321_*1338del	NP_001338426.1:n.*1321_*1338del
NM_001351498.1:c.*1499_*1516del	NP_001338427.1:n.*1499_*1516del
NM_001351499.1:c.*1321_*1338del	NP_001338428.1:n.*1321_*1338del
NM_001351500.1:c.*1321_*1338del	NP_001338429.1:n.*1321_*1338del
NM_001351501.1:c.*1321_*1338del	NP_001338430.1:n.*1321_*1338del
NM_001351502.1:c.*1321_*1338del	NP_001338431.1:n.*1321_*1338del
NR_147213.1:n.2831_2848del
NR_147214.1:n.3003_3020del
XM_011518391.2:c.*1499_*1516del	XP_011516693.1:n.*1499_*1516del
XM_017014464.1:c.1270+1437_1270+1454del	XP_016869953.1:n.1270+1437_1270+1454del
XM_017014465.1:c.1270+1437_1270+1454del	XP_016869954.1:n.1270+1437_1270+1454del
XM_017014467.1:c.*1321_*1338del	XP_016869956.1:n.*1321_*1338del
XM_017014468.1:c.*1321_*1338del	XP_016869957.1:n.*1321_*1338del
XM_017014469.1:c.1270+1437_1270+1454del	XP_016869958.1:n.1270+1437_1270+1454del
XM_017014470.1:c.1270+1437_1270+1454del	XP_016869959.1:n.1270+1437_1270+1454del
XR_001746242.2:n.1837+1437_1837+1454del
XR_001746244.2:n.1665+1437_1665+1454del
XR_001746245.1:n.3093_3110del
XR_001746248.1:n.4186_4203del
XR_002956770.1:n.2949_2966del
NM_001079802.2:c.*1321_*1338del MANE Select	NP_001073270.1:n.*1321_*1338del
NM_001198963.2:c.1270+1437_1270+1454del	NP_001185892.1:n.1270+1437_1270+1454del
NM_001351496.2:c.*1321_*1338del	NP_001338425.1:n.*1321_*1338del
NM_001351497.2:c.*1321_*1338del	NP_001338426.1:n.*1321_*1338del
NM_001351498.2:c.*1499_*1516del	NP_001338427.1:n.*1499_*1516del
NM_001351499.2:c.*1321_*1338del	NP_001338428.1:n.*1321_*1338del
NM_001351500.2:c.*1321_*1338del	NP_001338429.1:n.*1321_*1338del
NM_001351501.2:c.*1321_*1338del	NP_001338430.1:n.*1321_*1338del
NM_001351502.2:c.*1321_*1338del	NP_001338431.1:n.*1321_*1338del
NR_147213.2:n.2830_2847del
NR_147214.2:n.3002_3019del