Canonical Allele Identifier: CA295348

Gene: FKTN

Linked Data

• ClinVar Variation Id: 162564
• ClinVar RCV Id: RCV000149970 ; RCV001169642 ; RCV001169643
• dbSNP Id: rs188804693
• gnomAD v2: 9-108337237-A-G
• gnomAD v3: 9-105574956-A-G
• gnomAD v4: 9-105574956-A-G
• MyVariant Identifiers: chr9:g.108337237A>G (hg19) ; chr9:g.105574956A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.105574956A>G , CM000671.2:g.105574956A>G	GRCh38
NC_000009.11:g.108337237A>G , CM000671.1:g.108337237A>G	GRCh37
NC_000009.10:g.107377058A>G	NCBI36
NG_008754.1:g.21827A>G , LRG_434:g.21827A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357998.10:c.-77A>G MANE Select	ENSP00000350687.6:n.-77A>G
ENST00000602661.6:c.-77A>G	ENSP00000473540.2:n.-77A>G
ENST00000674563.1:c.-77A>G	ENSP00000502153.1:n.-77A>G
ENST00000675232.1:c.-77A>G	ENSP00000502043.1:n.-77A>G
ENST00000675443.1:c.-77A>G	ENSP00000502643.1:n.-77A>G
ENST00000675668.1:c.-77A>G	ENSP00000502113.1:n.-77A>G
ENST00000675695.1:c.-77A>G	ENSP00000502460.1:n.-77A>G
ENST00000675736.1:c.-77A>G	ENSP00000502809.1:n.-77A>G
ENST00000676192.1:c.-77A>G	ENSP00000502158.1:n.-77A>G
ENST00000223528.6:c.-77A>G	ENSP00000223528.2:n.-77A>G
ENST00000357998.9:c.-77A>G	ENSP00000350687.5:n.-77A>G
ENST00000448551.6:c.-77A>G	ENSP00000399140.2:n.-77A>G
ENST00000479846.1:n.255A>G
ENST00000490134.1:n.37A>G
ENST00000602661.5:c.-77A>G	ENSP00000473540.1:n.-77A>G
NM_001079802.1:c.-77A>G , LRG_434t1:c.-77A>G	NP_001073270.1:n.-77A>G
NM_001198963.1:c.-77A>G	NP_001185892.1:n.-77A>G
NM_006731.2:c.-77A>G , LRG_434t2:c.-77A>G	NP_006722.2:n.-77A>G
XM_006717014.2:c.-77A>G	XP_006717077.1:n.-77A>G
XM_011518368.1:c.-77A>G	XP_011516670.1:n.-77A>G
XM_011518369.1:c.-77A>G	XP_011516671.1:n.-77A>G
XM_011518370.1:c.-77A>G	XP_011516672.1:n.-77A>G
XM_011518371.1:c.-77A>G	XP_011516673.1:n.-77A>G
XM_011518372.1:c.-77A>G	XP_011516674.1:n.-77A>G
XM_011518373.1:c.-77A>G	XP_011516675.1:n.-77A>G
XM_011518374.1:c.-77A>G	XP_011516676.1:n.-77A>G
XM_011518375.1:c.-77A>G	XP_011516677.1:n.-77A>G
XM_011518376.1:c.-77A>G	XP_011516678.1:n.-77A>G
XM_011518377.1:c.-77A>G	XP_011516679.1:n.-77A>G
XM_011518378.1:c.-77A>G	XP_011516680.1:n.-77A>G
XM_011518380.1:c.-77A>G	XP_011516682.1:n.-77A>G
XM_011518381.1:c.-334A>G	XP_011516683.1:n.-334A>G
XM_011518386.1:c.-77A>G	XP_011516688.1:n.-77A>G
XM_011518387.1:c.-77A>G	XP_011516689.1:n.-77A>G
XM_011518388.1:c.-77A>G	XP_011516690.1:n.-77A>G
XM_011518389.1:c.-77A>G	XP_011516691.1:n.-77A>G
XM_011518391.1:c.-77A>G	XP_011516693.1:n.-77A>G
NM_001351496.1:c.-77A>G	NP_001338425.1:n.-77A>G
NM_001351497.1:c.-244A>G	NP_001338426.1:n.-244A>G
NM_001351498.1:c.-77A>G	NP_001338427.1:n.-77A>G
NM_001351499.1:c.-591A>G	NP_001338428.1:n.-591A>G
NM_001351500.1:c.-591A>G	NP_001338429.1:n.-591A>G
NM_001351501.1:c.-591A>G	NP_001338430.1:n.-591A>G
NM_001351502.1:c.-591A>G	NP_001338431.1:n.-591A>G
NR_147213.1:n.140A>G
NR_147214.1:n.48A>G
XM_011518368.2:c.-77A>G	XP_011516670.1:n.-77A>G
XM_011518369.2:c.-77A>G	XP_011516671.1:n.-77A>G
XM_011518370.2:c.-77A>G	XP_011516672.1:n.-77A>G
XM_011518371.2:c.-77A>G	XP_011516673.1:n.-77A>G
XM_011518373.2:c.-77A>G	XP_011516675.1:n.-77A>G
XM_011518374.2:c.-77A>G	XP_011516676.1:n.-77A>G
XM_011518375.2:c.-77A>G	XP_011516677.1:n.-77A>G
XM_011518376.2:c.-77A>G	XP_011516678.1:n.-77A>G
XM_011518378.2:c.-77A>G	XP_011516680.1:n.-77A>G
XM_011518381.3:c.-334A>G	XP_011516683.1:n.-334A>G
XM_011518387.2:c.-77A>G	XP_011516689.1:n.-77A>G
XM_011518391.2:c.-77A>G	XP_011516693.1:n.-77A>G
XM_017014462.1:c.-77A>G	XP_016869951.1:n.-77A>G
XM_017014463.1:c.-77A>G	XP_016869952.1:n.-77A>G
XM_017014464.1:c.-77A>G	XP_016869953.1:n.-77A>G
XM_017014465.1:c.-77A>G	XP_016869954.1:n.-77A>G
XM_017014467.1:c.-77A>G	XP_016869956.1:n.-77A>G
XM_017014468.1:c.-77A>G	XP_016869957.1:n.-77A>G
XM_017014469.1:c.-77A>G	XP_016869958.1:n.-77A>G
XM_017014470.1:c.-77A>G	XP_016869959.1:n.-77A>G
XM_017014472.2:c.-387A>G	XP_016869961.1:n.-387A>G
XM_017014475.1:c.-77A>G	XP_016869964.1:n.-77A>G
XR_001746242.2:n.288A>G
XR_001746243.2:n.288A>G
XR_001746244.2:n.288A>G
XR_001746245.1:n.138A>G
XR_001746248.1:n.1113A>G
XR_002956770.1:n.138A>G
NM_001079802.2:c.-77A>G MANE Select	NP_001073270.1:n.-77A>G
NM_001198963.2:c.-77A>G	NP_001185892.1:n.-77A>G
NM_001351496.2:c.-77A>G	NP_001338425.1:n.-77A>G
NM_001351497.2:c.-244A>G	NP_001338426.1:n.-244A>G
NM_001351498.2:c.-77A>G	NP_001338427.1:n.-77A>G
NM_001351499.2:c.-591A>G	NP_001338428.1:n.-591A>G
NM_001351500.2:c.-591A>G	NP_001338429.1:n.-591A>G
NM_001351501.2:c.-591A>G	NP_001338430.1:n.-591A>G
NM_001351502.2:c.-591A>G	NP_001338431.1:n.-591A>G
NR_147213.2:n.139A>G
NR_147214.2:n.47A>G