Canonical Allele Identifier: CA2691078572

Gene: FKTN

Linked Data

• gnomAD v4: 9-105640332-CTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.105640333_105640334del , CM000671.2:g.105640333_105640334del	GRCh38
NC_000009.11:g.108402614_108402615del , CM000671.1:g.108402614_108402615del	GRCh37
NC_000009.10:g.107442435_107442436del	NCBI36
NG_008754.1:g.87204_87205del , LRG_434:g.87204_87205del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357998.10:c.*5069_*5070del MANE Select	ENSP00000350687.6:n.*5069_*5070del
ENST00000642952.1:c.1843_1844del	ENSP00000493886.1:n.1843_1844del
ENST00000644273.1:c.786_787del
ENST00000674633.1:c.1271-4371_1271-4370del	ENSP00000502164.1:n.1271-4371_1271-4370del
ENST00000675695.1:c.*5436_*5437del	ENSP00000502460.1:n.*5436_*5437del
ENST00000676310.1:c.1270+5185_1270+5186del	ENSP00000501585.1:n.1270+5185_1270+5186del
ENST00000223528.6:c.*5069_*5070del	ENSP00000223528.2:n.*5069_*5070del
ENST00000357998.9:c.*210_*211del	ENSP00000350687.5:n.*210_*211del
ENST00000602526.1:c.*6493_*6494del	ENSP00000473347.1:n.*6493_*6494del
NM_001079802.1:c.*5069_*5070del , LRG_434t1:c.*5069_*5070del	NP_001073270.1:n.*5069_*5070del
NM_001198963.1:c.*210_*211del	NP_001185892.1:n.*210_*211del
NM_006731.2:c.*5069_*5070del , LRG_434t2:c.*5069_*5070del	NP_006722.2:n.*5069_*5070del
XM_006717014.2:c.*5247_*5248del	XP_006717077.1:n.*5247_*5248del
NM_001351496.1:c.*5069_*5070del	NP_001338425.1:n.*5069_*5070del
NM_001351497.1:c.*5069_*5070del	NP_001338426.1:n.*5069_*5070del
NM_001351498.1:c.*5247_*5248del	NP_001338427.1:n.*5247_*5248del
NM_001351499.1:c.*5069_*5070del	NP_001338428.1:n.*5069_*5070del
NM_001351500.1:c.*5069_*5070del	NP_001338429.1:n.*5069_*5070del
NM_001351501.1:c.*5069_*5070del	NP_001338430.1:n.*5069_*5070del
NM_001351502.1:c.*5069_*5070del	NP_001338431.1:n.*5069_*5070del
NR_147213.1:n.6579_6580del
NR_147214.1:n.6751_6752del
XM_011518391.2:c.*5247_*5248del	XP_011516693.1:n.*5247_*5248del
XM_017014464.1:c.1271-5132_1271-5131del	XP_016869953.1:n.1271-5132_1271-5131del
XM_017014465.1:c.1271-5132_1271-5131del	XP_016869954.1:n.1271-5132_1271-5131del
XM_017014467.1:c.*5069_*5070del	XP_016869956.1:n.*5069_*5070del
XM_017014468.1:c.*5069_*5070del	XP_016869957.1:n.*5069_*5070del
XM_017014469.1:c.1271-5132_1271-5131del	XP_016869958.1:n.1271-5132_1271-5131del
XM_017014470.1:c.1271-4371_1271-4370del	XP_016869959.1:n.1271-4371_1271-4370del
XR_001746242.2:n.1838-5132_1838-5131del
XR_001746244.2:n.1666-5132_1666-5131del
XR_001746245.1:n.6841_6842del
XR_001746248.1:n.7934_7935del
XR_002956770.1:n.6697_6698del
NM_001079802.2:c.*5069_*5070del MANE Select	NP_001073270.1:n.*5069_*5070del
NM_001198963.2:c.*210_*211del	NP_001185892.1:n.*210_*211del
NM_001351496.2:c.*5069_*5070del	NP_001338425.1:n.*5069_*5070del
NM_001351497.2:c.*5069_*5070del	NP_001338426.1:n.*5069_*5070del
NM_001351498.2:c.*5247_*5248del	NP_001338427.1:n.*5247_*5248del
NM_001351499.2:c.*5069_*5070del	NP_001338428.1:n.*5069_*5070del
NM_001351500.2:c.*5069_*5070del	NP_001338429.1:n.*5069_*5070del
NM_001351501.2:c.*5069_*5070del	NP_001338430.1:n.*5069_*5070del
NM_001351502.2:c.*5069_*5070del	NP_001338431.1:n.*5069_*5070del
NR_147213.2:n.6578_6579del
NR_147214.2:n.6750_6751del