Canonical Allele Identifier: CA1870288494

Gene: FKTN

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.105637600_105637601delinsTC , CM000671.2:g.105637600_105637601delinsTC	GRCh38
NC_000009.11:g.108399881_108399882delinsTC , CM000671.1:g.108399881_108399882delinsTC	GRCh37
NC_000009.10:g.107439702_107439703delinsTC	NCBI36
NG_008754.1:g.84471_84472delinsTC , LRG_434:g.84471_84472delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357998.10:c.*2336_*2337delinsTC MANE Select	ENSP00000350687.6:n.*2336_*2337delinsTC
ENST00000642952.1:c.1610+2452_1610+2453delinsTC	ENSP00000493886.1:n.1610+2452_1610+2453delinsTC
ENST00000644273.1:c.553+2452_553+2453delinsTC
ENST00000674633.1:c.1270+2452_1270+2453delinsTC	ENSP00000502164.1:n.1270+2452_1270+2453delinsTC
ENST00000675695.1:c.*2703_*2704delinsTC	ENSP00000502460.1:n.*2703_*2704delinsTC
ENST00000675736.1:c.*3502_*3503delinsTC	ENSP00000502809.1:n.*3502_*3503delinsTC
ENST00000676011.1:n.5086_5087delinsTC
ENST00000676310.1:c.1270+2452_1270+2453delinsTC	ENSP00000501585.1:n.1270+2452_1270+2453delinsTC
ENST00000223528.6:c.*2336_*2337delinsTC	ENSP00000223528.2:n.*2336_*2337delinsTC
ENST00000357998.9:c.1270+2452_1270+2453delinsTC	ENSP00000350687.5:n.1270+2452_1270+2453delinsTC
ENST00000448551.6:c.1270+2452_1270+2453delinsTC	ENSP00000399140.2:n.1270+2452_1270+2453delinsTC
ENST00000602526.1:c.*3760_*3761delinsTC	ENSP00000473347.1:n.*3760_*3761delinsTC
NM_001079802.1:c.*2336_*2337delinsTC , LRG_434t1:c.*2336_*2337delinsTC	NP_001073270.1:n.*2336_*2337delinsTC
NM_001198963.1:c.1270+2452_1270+2453delinsTC	NP_001185892.1:n.1270+2452_1270+2453delinsTC
NM_006731.2:c.*2336_*2337delinsTC , LRG_434t2:c.*2336_*2337delinsTC	NP_006722.2:n.*2336_*2337delinsTC
XM_006717014.2:c.*2514_*2515delinsTC	XP_006717077.1:n.*2514_*2515delinsTC
NM_001351496.1:c.*2336_*2337delinsTC	NP_001338425.1:n.*2336_*2337delinsTC
NM_001351497.1:c.*2336_*2337delinsTC	NP_001338426.1:n.*2336_*2337delinsTC
NM_001351498.1:c.*2514_*2515delinsTC	NP_001338427.1:n.*2514_*2515delinsTC
NM_001351499.1:c.*2336_*2337delinsTC	NP_001338428.1:n.*2336_*2337delinsTC
NM_001351500.1:c.*2336_*2337delinsTC	NP_001338429.1:n.*2336_*2337delinsTC
NM_001351501.1:c.*2336_*2337delinsTC	NP_001338430.1:n.*2336_*2337delinsTC
NM_001351502.1:c.*2336_*2337delinsTC	NP_001338431.1:n.*2336_*2337delinsTC
NR_147213.1:n.3846_3847delinsTC
NR_147214.1:n.4018_4019delinsTC
XM_011518391.2:c.*2514_*2515delinsTC	XP_011516693.1:n.*2514_*2515delinsTC
XM_017014464.1:c.1270+2452_1270+2453delinsTC	XP_016869953.1:n.1270+2452_1270+2453delinsTC
XM_017014465.1:c.1270+2452_1270+2453delinsTC	XP_016869954.1:n.1270+2452_1270+2453delinsTC
XM_017014467.1:c.*2336_*2337delinsTC	XP_016869956.1:n.*2336_*2337delinsTC
XM_017014468.1:c.*2336_*2337delinsTC	XP_016869957.1:n.*2336_*2337delinsTC
XM_017014469.1:c.1270+2452_1270+2453delinsTC	XP_016869958.1:n.1270+2452_1270+2453delinsTC
XM_017014470.1:c.1270+2452_1270+2453delinsTC	XP_016869959.1:n.1270+2452_1270+2453delinsTC
XR_001746242.2:n.1837+2452_1837+2453delinsTC
XR_001746244.2:n.1665+2452_1665+2453delinsTC
XR_001746245.1:n.4108_4109delinsTC
XR_001746248.1:n.5201_5202delinsTC
XR_002956770.1:n.3964_3965delinsTC
NM_001079802.2:c.*2336_*2337delinsTC MANE Select	NP_001073270.1:n.*2336_*2337delinsTC
NM_001198963.2:c.1270+2452_1270+2453delinsTC	NP_001185892.1:n.1270+2452_1270+2453delinsTC
NM_001351496.2:c.*2336_*2337delinsTC	NP_001338425.1:n.*2336_*2337delinsTC
NM_001351497.2:c.*2336_*2337delinsTC	NP_001338426.1:n.*2336_*2337delinsTC
NM_001351498.2:c.*2514_*2515delinsTC	NP_001338427.1:n.*2514_*2515delinsTC
NM_001351499.2:c.*2336_*2337delinsTC	NP_001338428.1:n.*2336_*2337delinsTC
NM_001351500.2:c.*2336_*2337delinsTC	NP_001338429.1:n.*2336_*2337delinsTC
NM_001351501.2:c.*2336_*2337delinsTC	NP_001338430.1:n.*2336_*2337delinsTC
NM_001351502.2:c.*2336_*2337delinsTC	NP_001338431.1:n.*2336_*2337delinsTC
NR_147213.2:n.3845_3846delinsTC
NR_147214.2:n.4017_4018delinsTC