Canonical Allele Identifier: CA858144972

Gene: FKTN

Linked Data

• dbSNP Id: rs1383609308
• gnomAD v3: 9-105640396-C-CA
• gnomAD v4: 9-105640396-C-CA
• MyVariant Identifiers: chr9:g.108402677_108402678insA (hg19) ; chr9:g.105640396_105640397insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.105640403dup , CM000671.2:g.105640403dup	GRCh38
NC_000009.11:g.108402684dup , CM000671.1:g.108402684dup	GRCh37
NC_000009.10:g.107442505dup	NCBI36
NG_008754.1:g.87274dup , LRG_434:g.87274dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357998.10:c.*5139dup MANE Select	ENSP00000350687.6:n.*5139dup
ENST00000642952.1:c.1913dup	ENSP00000493886.1:n.1913dup
ENST00000644273.1:c.856dup
ENST00000674633.1:c.1271-4301dup	ENSP00000502164.1:n.1271-4301dup
ENST00000675695.1:c.*5506dup	ENSP00000502460.1:n.*5506dup
ENST00000676310.1:c.1270+5255dup	ENSP00000501585.1:n.1270+5255dup
ENST00000223528.6:c.*5139dup	ENSP00000223528.2:n.*5139dup
ENST00000357998.9:c.*280dup	ENSP00000350687.5:n.*280dup
ENST00000602526.1:c.*6563dup	ENSP00000473347.1:n.*6563dup
NM_001079802.1:c.*5139dup , LRG_434t1:c.*5139dup	NP_001073270.1:n.*5139dup
NM_001198963.1:c.*280dup	NP_001185892.1:n.*280dup
NM_006731.2:c.*5139dup , LRG_434t2:c.*5139dup	NP_006722.2:n.*5139dup
XM_006717014.2:c.*5317dup	XP_006717077.1:n.*5317dup
NM_001351496.1:c.*5139dup	NP_001338425.1:n.*5139dup
NM_001351497.1:c.*5139dup	NP_001338426.1:n.*5139dup
NM_001351498.1:c.*5317dup	NP_001338427.1:n.*5317dup
NM_001351499.1:c.*5139dup	NP_001338428.1:n.*5139dup
NM_001351500.1:c.*5139dup	NP_001338429.1:n.*5139dup
NM_001351501.1:c.*5139dup	NP_001338430.1:n.*5139dup
NM_001351502.1:c.*5139dup	NP_001338431.1:n.*5139dup
NR_147213.1:n.6649dup
NR_147214.1:n.6821dup
XM_011518391.2:c.*5317dup	XP_011516693.1:n.*5317dup
XM_017014464.1:c.1271-5062dup	XP_016869953.1:n.1271-5062dup
XM_017014465.1:c.1271-5062dup	XP_016869954.1:n.1271-5062dup
XM_017014467.1:c.*5139dup	XP_016869956.1:n.*5139dup
XM_017014468.1:c.*5139dup	XP_016869957.1:n.*5139dup
XM_017014469.1:c.1271-5062dup	XP_016869958.1:n.1271-5062dup
XM_017014470.1:c.1271-4301dup	XP_016869959.1:n.1271-4301dup
XR_001746242.2:n.1838-5062dup
XR_001746244.2:n.1666-5062dup
XR_001746245.1:n.6911dup
XR_001746248.1:n.8004dup
XR_002956770.1:n.6767dup
NM_001079802.2:c.*5139dup MANE Select	NP_001073270.1:n.*5139dup
NM_001198963.2:c.*280dup	NP_001185892.1:n.*280dup
NM_001351496.2:c.*5139dup	NP_001338425.1:n.*5139dup
NM_001351497.2:c.*5139dup	NP_001338426.1:n.*5139dup
NM_001351498.2:c.*5317dup	NP_001338427.1:n.*5317dup
NM_001351499.2:c.*5139dup	NP_001338428.1:n.*5139dup
NM_001351500.2:c.*5139dup	NP_001338429.1:n.*5139dup
NM_001351501.2:c.*5139dup	NP_001338430.1:n.*5139dup
NM_001351502.2:c.*5139dup	NP_001338431.1:n.*5139dup
NR_147213.2:n.6648dup
NR_147214.2:n.6820dup