Canonical Allele Identifier: CA858142726

Gene: FKTN

Linked Data

• dbSNP Id: rs1374852895
• MyVariant Identifiers: chr9:g.108398461_108398462insCCAATTT (hg19) ; chr9:g.105636180_105636181insCCAATTT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.105636181_105636187dup , CM000671.2:g.105636181_105636187dup	GRCh38
NC_000009.11:g.108398462_108398468dup , CM000671.1:g.108398462_108398468dup	GRCh37
NC_000009.10:g.107438283_107438289dup	NCBI36
NG_008754.1:g.83052_83058dup , LRG_434:g.83052_83058dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357998.10:c.*917_*923dup MANE Select	ENSP00000350687.6:n.*917_*923dup
ENST00000602661.6:c.*1911_*1917dup	ENSP00000473540.2:n.*1911_*1917dup
ENST00000642177.1:c.*486-492_*486-486dup	ENSP00000495864.1:n.*486-492_*486-486dup
ENST00000642537.1:c.*1539-492_*1539-486dup	ENSP00000495945.1:n.*1539-492_*1539-486dup
ENST00000642952.1:c.1610+1033_1610+1039dup	ENSP00000493886.1:n.1610+1033_1610+1039dup
ENST00000644273.1:c.553+1033_553+1039dup
ENST00000645933.1:c.*1584-492_*1584-486dup	ENSP00000495852.1:n.*1584-492_*1584-486dup
ENST00000674563.1:c.*1284_*1290dup	ENSP00000502153.1:n.*1284_*1290dup
ENST00000674633.1:c.1270+1033_1270+1039dup	ENSP00000502164.1:n.1270+1033_1270+1039dup
ENST00000675695.1:c.*1284_*1290dup	ENSP00000502460.1:n.*1284_*1290dup
ENST00000675736.1:c.*2083_*2089dup	ENSP00000502809.1:n.*2083_*2089dup
ENST00000676011.1:n.3667_3673dup
ENST00000676310.1:c.1270+1033_1270+1039dup	ENSP00000501585.1:n.1270+1033_1270+1039dup
ENST00000223528.6:c.*917_*923dup	ENSP00000223528.2:n.*917_*923dup
ENST00000357998.9:c.1270+1033_1270+1039dup	ENSP00000350687.5:n.1270+1033_1270+1039dup
ENST00000448551.6:c.1270+1033_1270+1039dup	ENSP00000399140.2:n.1270+1033_1270+1039dup
ENST00000457847.1:c.361-492_361-486dup
ENST00000602526.1:c.*2341_*2347dup	ENSP00000473347.1:n.*2341_*2347dup
ENST00000602661.5:c.*917_*923dup	ENSP00000473540.1:n.*917_*923dup
NM_001079802.1:c.*917_*923dup , LRG_434t1:c.*917_*923dup	NP_001073270.1:n.*917_*923dup
NM_001198963.1:c.1270+1033_1270+1039dup	NP_001185892.1:n.1270+1033_1270+1039dup
NM_006731.2:c.*917_*923dup , LRG_434t2:c.*917_*923dup	NP_006722.2:n.*917_*923dup
XM_006717014.2:c.*1095_*1101dup	XP_006717077.1:n.*1095_*1101dup
NM_001351496.1:c.*917_*923dup	NP_001338425.1:n.*917_*923dup
NM_001351497.1:c.*917_*923dup	NP_001338426.1:n.*917_*923dup
NM_001351498.1:c.*1095_*1101dup	NP_001338427.1:n.*1095_*1101dup
NM_001351499.1:c.*917_*923dup	NP_001338428.1:n.*917_*923dup
NM_001351500.1:c.*917_*923dup	NP_001338429.1:n.*917_*923dup
NM_001351501.1:c.*917_*923dup	NP_001338430.1:n.*917_*923dup
NM_001351502.1:c.*917_*923dup	NP_001338431.1:n.*917_*923dup
NR_147213.1:n.2427_2433dup
NR_147214.1:n.2599_2605dup
XM_011518391.2:c.*1095_*1101dup	XP_011516693.1:n.*1095_*1101dup
XM_017014464.1:c.1270+1033_1270+1039dup	XP_016869953.1:n.1270+1033_1270+1039dup
XM_017014465.1:c.1270+1033_1270+1039dup	XP_016869954.1:n.1270+1033_1270+1039dup
XM_017014467.1:c.*917_*923dup	XP_016869956.1:n.*917_*923dup
XM_017014468.1:c.*917_*923dup	XP_016869957.1:n.*917_*923dup
XM_017014469.1:c.1270+1033_1270+1039dup	XP_016869958.1:n.1270+1033_1270+1039dup
XM_017014470.1:c.1270+1033_1270+1039dup	XP_016869959.1:n.1270+1033_1270+1039dup
XR_001746242.2:n.1837+1033_1837+1039dup
XR_001746244.2:n.1665+1033_1665+1039dup
XR_001746245.1:n.2689_2695dup
XR_001746248.1:n.3782_3788dup
XR_002956770.1:n.2545_2551dup
NM_001079802.2:c.*917_*923dup MANE Select	NP_001073270.1:n.*917_*923dup
NM_001198963.2:c.1270+1033_1270+1039dup	NP_001185892.1:n.1270+1033_1270+1039dup
NM_001351496.2:c.*917_*923dup	NP_001338425.1:n.*917_*923dup
NM_001351497.2:c.*917_*923dup	NP_001338426.1:n.*917_*923dup
NM_001351498.2:c.*1095_*1101dup	NP_001338427.1:n.*1095_*1101dup
NM_001351499.2:c.*917_*923dup	NP_001338428.1:n.*917_*923dup
NM_001351500.2:c.*917_*923dup	NP_001338429.1:n.*917_*923dup
NM_001351501.2:c.*917_*923dup	NP_001338430.1:n.*917_*923dup
NM_001351502.2:c.*917_*923dup	NP_001338431.1:n.*917_*923dup
NR_147213.2:n.2426_2432dup
NR_147214.2:n.2598_2604dup