Canonical Allele Identifier: CA658822041

Gene: FKTN

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.105635142_105635164del , CM000671.2:g.105635142_105635164del	GRCh38
NC_000009.11:g.108397423_108397445del , CM000671.1:g.108397423_108397445del	GRCh37
NC_000009.10:g.107437244_107437266del	NCBI36
NG_008754.1:g.82013_82035del , LRG_434:g.82013_82035del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357998.10:c.1264_1286del MANE Select	ENSP00000350687.6:p.Asn422SerfsTer24
ENST00000602661.6:c.*872_*894del	ENSP00000473540.2:n.*872_*894del
ENST00000642177.1:c.*479_*485+16del
ENST00000642537.1:c.*1532_*1538+16del
ENST00000642952.1:c.1604_1610+16del
ENST00000644273.1:c.547_553+16del
ENST00000645933.1:c.*1577_*1583+16del
ENST00000674563.1:c.*245_*267del	ENSP00000502153.1:n.*245_*267del
ENST00000674633.1:c.1264_1270+16del
ENST00000675695.1:c.*245_*267del	ENSP00000502460.1:n.*245_*267del
ENST00000675736.1:c.*1044_*1066del	ENSP00000502809.1:n.*1044_*1066del
ENST00000676011.1:n.2628_2650del
ENST00000676310.1:c.1264_1270+16del
ENST00000223528.6:c.1264_1286del	ENSP00000223528.2:p.Asn422SerfsTer24
ENST00000357998.9:c.1264_1270+16del
ENST00000448551.6:c.1264_1270+16del
ENST00000457847.1:c.354_360+16del
ENST00000602526.1:c.*1302_*1324del	ENSP00000473347.1:n.*1302_*1324del
ENST00000602661.5:c.1264_1286del	ENSP00000473540.1:p.Asn422SerfsTer24
NM_001079802.1:c.1264_1286del , LRG_434t1:c.1264_1286del	NP_001073270.1:p.Asn422SerfsTer24
NM_001198963.1:c.1264_1270+16del
NM_006731.2:c.1264_1286del , LRG_434t2:c.1264_1286del	NP_006722.2:p.Asn422SerfsTer24
XM_006717014.2:c.*56_*78del	XP_006717077.1:n.*56_*78del
XM_011518378.1:c.*48_*70del	XP_011516680.1:n.*48_*70del
XM_011518386.1:c.*56_*78del	XP_011516688.1:n.*56_*78del
XM_011518391.1:c.*56_*78del	XP_011516693.1:n.*56_*78del
NM_001351496.1:c.1264_1286del	NP_001338425.1:p.Asn422SerfsTer24
NM_001351497.1:c.1195_1217del	NP_001338426.1:p.Asn399SerfsTer24
NM_001351498.1:c.*56_*78del	NP_001338427.1:n.*56_*78del
NM_001351499.1:c.868_890del	NP_001338428.1:p.Asn290SerfsTer24
NM_001351500.1:c.868_890del	NP_001338429.1:p.Asn290SerfsTer24
NM_001351501.1:c.868_890del	NP_001338430.1:p.Asn290SerfsTer24
NM_001351502.1:c.868_890del	NP_001338431.1:p.Asn290SerfsTer24
NR_147213.1:n.1388_1410del
NR_147214.1:n.1560_1582del
XM_011518378.2:c.*48_*70del	XP_011516680.1:n.*48_*70del
XM_011518391.2:c.*56_*78del	XP_011516693.1:n.*56_*78del
XM_017014464.1:c.1264_1270+16del
XM_017014465.1:c.1264_1270+16del
XM_017014467.1:c.1264_1286del	XP_016869956.1:p.Asn422SerfsTer24
XM_017014468.1:c.1264_1286del	XP_016869957.1:p.Asn422SerfsTer24
XM_017014469.1:c.1264_1270+16del
XM_017014470.1:c.1264_1270+16del
XR_001746242.2:n.1831_1837+16del
XR_001746244.2:n.1659_1665+16del
XR_001746245.1:n.1650_1672del
XR_001746248.1:n.2743_2765del
XR_002956770.1:n.1506_1528del
NM_001079802.2:c.1264_1286del MANE Select	NP_001073270.1:p.Asn422SerfsTer24
NM_001198963.2:c.1264_1270+16del
NM_001351496.2:c.1264_1286del	NP_001338425.1:p.Asn422SerfsTer24
NM_001351497.2:c.1195_1217del	NP_001338426.1:p.Asn399SerfsTer24
NM_001351498.2:c.*56_*78del	NP_001338427.1:n.*56_*78del
NM_001351499.2:c.868_890del	NP_001338428.1:p.Asn290SerfsTer24
NM_001351500.2:c.868_890del	NP_001338429.1:p.Asn290SerfsTer24
NM_001351501.2:c.868_890del	NP_001338430.1:p.Asn290SerfsTer24
NM_001351502.2:c.868_890del	NP_001338431.1:p.Asn290SerfsTer24
NR_147213.2:n.1387_1409del
NR_147214.2:n.1559_1581del