Canonical Allele Identifier: CA2691078586

Gene: FKTN

Linked Data

• gnomAD v4: 9-105640343-G-GAC

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.105640344_105640345insCA , CM000671.2:g.105640344_105640345insCA	GRCh38
NC_000009.11:g.108402625_108402626insCA , CM000671.1:g.108402625_108402626insCA	GRCh37
NC_000009.10:g.107442446_107442447insCA	NCBI36
NG_008754.1:g.87215_87216insCA , LRG_434:g.87215_87216insCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357998.10:c.*5080_*5081insCA MANE Select	ENSP00000350687.6:n.*5080_*5081insCA
ENST00000642952.1:c.1854_1855insCA	ENSP00000493886.1:n.1854_1855insCA
ENST00000644273.1:c.797_798insCA
ENST00000674633.1:c.1271-4360_1271-4359insCA	ENSP00000502164.1:n.1271-4360_1271-4359insCA
ENST00000675695.1:c.*5447_*5448insCA	ENSP00000502460.1:n.*5447_*5448insCA
ENST00000676310.1:c.1270+5196_1270+5197insCA	ENSP00000501585.1:n.1270+5196_1270+5197insCA
ENST00000223528.6:c.*5080_*5081insCA	ENSP00000223528.2:n.*5080_*5081insCA
ENST00000357998.9:c.*221_*222insCA	ENSP00000350687.5:n.*221_*222insCA
ENST00000602526.1:c.*6504_*6505insCA	ENSP00000473347.1:n.*6504_*6505insCA
NM_001079802.1:c.*5080_*5081insCA , LRG_434t1:c.*5080_*5081insCA	NP_001073270.1:n.*5080_*5081insCA
NM_001198963.1:c.*221_*222insCA	NP_001185892.1:n.*221_*222insCA
NM_006731.2:c.*5080_*5081insCA , LRG_434t2:c.*5080_*5081insCA	NP_006722.2:n.*5080_*5081insCA
XM_006717014.2:c.*5258_*5259insCA	XP_006717077.1:n.*5258_*5259insCA
NM_001351496.1:c.*5080_*5081insCA	NP_001338425.1:n.*5080_*5081insCA
NM_001351497.1:c.*5080_*5081insCA	NP_001338426.1:n.*5080_*5081insCA
NM_001351498.1:c.*5258_*5259insCA	NP_001338427.1:n.*5258_*5259insCA
NM_001351499.1:c.*5080_*5081insCA	NP_001338428.1:n.*5080_*5081insCA
NM_001351500.1:c.*5080_*5081insCA	NP_001338429.1:n.*5080_*5081insCA
NM_001351501.1:c.*5080_*5081insCA	NP_001338430.1:n.*5080_*5081insCA
NM_001351502.1:c.*5080_*5081insCA	NP_001338431.1:n.*5080_*5081insCA
NR_147213.1:n.6590_6591insCA
NR_147214.1:n.6762_6763insCA
XM_011518391.2:c.*5258_*5259insCA	XP_011516693.1:n.*5258_*5259insCA
XM_017014464.1:c.1271-5121_1271-5120insCA	XP_016869953.1:n.1271-5121_1271-5120insCA
XM_017014465.1:c.1271-5121_1271-5120insCA	XP_016869954.1:n.1271-5121_1271-5120insCA
XM_017014467.1:c.*5080_*5081insCA	XP_016869956.1:n.*5080_*5081insCA
XM_017014468.1:c.*5080_*5081insCA	XP_016869957.1:n.*5080_*5081insCA
XM_017014469.1:c.1271-5121_1271-5120insCA	XP_016869958.1:n.1271-5121_1271-5120insCA
XM_017014470.1:c.1271-4360_1271-4359insCA	XP_016869959.1:n.1271-4360_1271-4359insCA
XR_001746242.2:n.1838-5121_1838-5120insCA
XR_001746244.2:n.1666-5121_1666-5120insCA
XR_001746245.1:n.6852_6853insCA
XR_001746248.1:n.7945_7946insCA
XR_002956770.1:n.6708_6709insCA
NM_001079802.2:c.*5080_*5081insCA MANE Select	NP_001073270.1:n.*5080_*5081insCA
NM_001198963.2:c.*221_*222insCA	NP_001185892.1:n.*221_*222insCA
NM_001351496.2:c.*5080_*5081insCA	NP_001338425.1:n.*5080_*5081insCA
NM_001351497.2:c.*5080_*5081insCA	NP_001338426.1:n.*5080_*5081insCA
NM_001351498.2:c.*5258_*5259insCA	NP_001338427.1:n.*5258_*5259insCA
NM_001351499.2:c.*5080_*5081insCA	NP_001338428.1:n.*5080_*5081insCA
NM_001351500.2:c.*5080_*5081insCA	NP_001338429.1:n.*5080_*5081insCA
NM_001351501.2:c.*5080_*5081insCA	NP_001338430.1:n.*5080_*5081insCA
NM_001351502.2:c.*5080_*5081insCA	NP_001338431.1:n.*5080_*5081insCA
NR_147213.2:n.6589_6590insCA
NR_147214.2:n.6761_6762insCA