Canonical Allele Identifier: CA590004086

Gene: FKTN

Linked Data

• dbSNP Id: rs1405496978
• gnomAD v2: 9-108400825-G-GCCTGTAT
• gnomAD v3: 9-105638544-G-GCCTGTAT
• gnomAD v4: 9-105638544-G-GCCTGTAT
• MyVariant Identifiers: chr9:g.108400825_108400826insCCTGTAT (hg19) ; chr9:g.105638544_105638545insCCTGTAT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.105638545_105638551dup , CM000671.2:g.105638545_105638551dup	GRCh38
NC_000009.11:g.108400826_108400832dup , CM000671.1:g.108400826_108400832dup	GRCh37
NC_000009.10:g.107440647_107440653dup	NCBI36
NG_008754.1:g.85416_85422dup , LRG_434:g.85416_85422dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357998.10:c.*3281_*3287dup MANE Select	ENSP00000350687.6:n.*3281_*3287dup
ENST00000642952.1:c.1611-1556_1611-1550dup	ENSP00000493886.1:n.1611-1556_1611-1550dup
ENST00000644273.1:c.554-1556_554-1550dup
ENST00000674633.1:c.1270+3397_1270+3403dup	ENSP00000502164.1:n.1270+3397_1270+3403dup
ENST00000675695.1:c.*3648_*3654dup	ENSP00000502460.1:n.*3648_*3654dup
ENST00000675736.1:c.*4447_*4453dup	ENSP00000502809.1:n.*4447_*4453dup
ENST00000676011.1:n.6031_6037dup
ENST00000676310.1:c.1270+3397_1270+3403dup	ENSP00000501585.1:n.1270+3397_1270+3403dup
ENST00000223528.6:c.*3281_*3287dup	ENSP00000223528.2:n.*3281_*3287dup
ENST00000357998.9:c.1271-1556_1271-1550dup	ENSP00000350687.5:n.1271-1556_1271-1550dup
ENST00000448551.6:c.1271-1556_1271-1550dup	ENSP00000399140.2:n.1271-1556_1271-1550dup
ENST00000602526.1:c.*4705_*4711dup	ENSP00000473347.1:n.*4705_*4711dup
NM_001079802.1:c.*3281_*3287dup , LRG_434t1:c.*3281_*3287dup	NP_001073270.1:n.*3281_*3287dup
NM_001198963.1:c.1271-1556_1271-1550dup	NP_001185892.1:n.1271-1556_1271-1550dup
NM_006731.2:c.*3281_*3287dup , LRG_434t2:c.*3281_*3287dup	NP_006722.2:n.*3281_*3287dup
XM_006717014.2:c.*3459_*3465dup	XP_006717077.1:n.*3459_*3465dup
NM_001351496.1:c.*3281_*3287dup	NP_001338425.1:n.*3281_*3287dup
NM_001351497.1:c.*3281_*3287dup	NP_001338426.1:n.*3281_*3287dup
NM_001351498.1:c.*3459_*3465dup	NP_001338427.1:n.*3459_*3465dup
NM_001351499.1:c.*3281_*3287dup	NP_001338428.1:n.*3281_*3287dup
NM_001351500.1:c.*3281_*3287dup	NP_001338429.1:n.*3281_*3287dup
NM_001351501.1:c.*3281_*3287dup	NP_001338430.1:n.*3281_*3287dup
NM_001351502.1:c.*3281_*3287dup	NP_001338431.1:n.*3281_*3287dup
NR_147213.1:n.4791_4797dup
NR_147214.1:n.4963_4969dup
XM_011518391.2:c.*3459_*3465dup	XP_011516693.1:n.*3459_*3465dup
XM_017014464.1:c.1270+3397_1270+3403dup	XP_016869953.1:n.1270+3397_1270+3403dup
XM_017014465.1:c.1270+3397_1270+3403dup	XP_016869954.1:n.1270+3397_1270+3403dup
XM_017014467.1:c.*3281_*3287dup	XP_016869956.1:n.*3281_*3287dup
XM_017014468.1:c.*3281_*3287dup	XP_016869957.1:n.*3281_*3287dup
XM_017014469.1:c.1270+3397_1270+3403dup	XP_016869958.1:n.1270+3397_1270+3403dup
XM_017014470.1:c.1270+3397_1270+3403dup	XP_016869959.1:n.1270+3397_1270+3403dup
XR_001746242.2:n.1837+3397_1837+3403dup
XR_001746244.2:n.1665+3397_1665+3403dup
XR_001746245.1:n.5053_5059dup
XR_001746248.1:n.6146_6152dup
XR_002956770.1:n.4909_4915dup
NM_001079802.2:c.*3281_*3287dup MANE Select	NP_001073270.1:n.*3281_*3287dup
NM_001198963.2:c.1271-1556_1271-1550dup	NP_001185892.1:n.1271-1556_1271-1550dup
NM_001351496.2:c.*3281_*3287dup	NP_001338425.1:n.*3281_*3287dup
NM_001351497.2:c.*3281_*3287dup	NP_001338426.1:n.*3281_*3287dup
NM_001351498.2:c.*3459_*3465dup	NP_001338427.1:n.*3459_*3465dup
NM_001351499.2:c.*3281_*3287dup	NP_001338428.1:n.*3281_*3287dup
NM_001351500.2:c.*3281_*3287dup	NP_001338429.1:n.*3281_*3287dup
NM_001351501.2:c.*3281_*3287dup	NP_001338430.1:n.*3281_*3287dup
NM_001351502.2:c.*3281_*3287dup	NP_001338431.1:n.*3281_*3287dup
NR_147213.2:n.4790_4796dup
NR_147214.2:n.4962_4968dup