Canonical Allele Identifier: CA5170377
Gene: FKTN HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs764125009

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.105601349G>C , CM000671.2:g.105601349G>C GRCh38
NC_000009.10:g.107403451G>C NCBI36
NC_000009.11:g.108363630G>C , CM000671.1:g.108363630G>C GRCh37
NG_008754.1:g.48220G>C , LRG_434:g.48220G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000223528.6:c.369+1G>C ENSP00000223528.2:p.=
ENST00000357998.9:c.369+1G>C ENSP00000350687.5:p.=
ENST00000374705.4:c.300+1G>C ENSP00000363837.4:p.=
ENST00000448551.6:c.369+1G>C ENSP00000399140.2:p.=
ENST00000602526.1:c.*289+1G>C ENSP00000473347.1:p.=
ENST00000602661.5:c.369+1G>C ENSP00000473540.1:p.=
NM_001079802.1:c.369+1G>C , LRG_434t1:c.369+1G>C NP_001073270.1:p.=
NM_001198963.1:c.369+1G>C NP_001185892.1:p.=
NM_006731.2:c.369+1G>C , LRG_434t2:c.369+1G>C NP_006722.2:p.=
XM_006717014.2:c.369+1G>C XP_006717077.1:p.=
XM_011518368.1:c.369+1G>C XP_011516670.1:p.=
XM_011518369.1:c.369+1G>C XP_011516671.1:p.=
XM_011518370.1:c.369+1G>C XP_011516672.1:p.=
XM_011518371.1:c.369+1G>C XP_011516673.1:p.=
XM_011518372.1:c.369+1G>C XP_011516674.1:p.=
XM_011518373.1:c.369+1G>C XP_011516675.1:p.=
XM_011518374.1:c.369+1G>C XP_011516676.1:p.=
XM_011518375.1:c.369+1G>C XP_011516677.1:p.=
XM_011518376.1:c.369+1G>C XP_011516678.1:p.=
XM_011518377.1:c.369+1G>C XP_011516679.1:p.=
XM_011518378.1:c.369+1G>C XP_011516680.1:p.=
XM_011518379.1:c.300+1G>C XP_011516681.1:p.=
XM_011518380.1:c.369+1G>C XP_011516682.1:p.=
XM_011518381.1:c.183+1G>C XP_011516683.1:p.=
XM_011518382.1:c.183+1G>C XP_011516684.1:p.=
XM_011518383.1:c.183+1G>C XP_011516685.1:p.=
XM_011518384.1:c.183+1G>C XP_011516686.1:p.=
XM_011518385.1:c.183+1G>C XP_011516687.1:p.=
XM_011518386.1:c.369+1G>C XP_011516688.1:p.=
XM_011518387.1:c.369+1G>C XP_011516689.1:p.=
XM_011518388.1:c.369+1G>C XP_011516690.1:p.=
XM_011518389.1:c.369+1G>C XP_011516691.1:p.=
XM_011518390.1:c.-125+1G>C XP_011516692.1:p.=
XM_011518391.1:c.369+1G>C XP_011516693.1:p.=