Canonical Allele Identifier: CA2521113470

Gene: FHOD3

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.36527561_36527562insCACTGCTACTA , CM000680.2:g.36527561_36527562insCACTGCTACTA	GRCh38
NC_000018.9:g.34107524_34107525insCACTGCTACTA , CM000680.1:g.34107524_34107525insCACTGCTACTA	GRCh37
NC_000018.8:g.32361522_32361523insCACTGCTACTA	NCBI36
NG_042837.1:g.234866_234867insCACTGCTACTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000590592.6:c.511+15018_511+15019insCACTGCTACTA MANE Select	ENSP00000466937.1:n.511+15018_511+15019insCACTGCTACTA
ENST00000257209.8:c.511+15018_511+15019insCACTGCTACTA	ENSP00000257209.3:n.511+15018_511+15019insCACTGCTACTA
ENST00000359247.8:c.511+15018_511+15019insCACTGCTACTA	ENSP00000352186.3:n.511+15018_511+15019insCACTGCTACTA
ENST00000589114.5:n.630+15018_630+15019insCACTGCTACTA
ENST00000590592.5:c.511+15018_511+15019insCACTGCTACTA	ENSP00000466937.1:n.511+15018_511+15019insCACTGCTACTA
NM_001281739.1:c.511+15018_511+15019insCACTGCTACTA	NP_001268668.1:n.511+15018_511+15019insCACTGCTACTA
NM_001281739.2:c.511+15018_511+15019insCACTGCTACTA	NP_001268668.1:n.511+15018_511+15019insCACTGCTACTA
NM_001281740.1:c.511+15018_511+15019insCACTGCTACTA	NP_001268669.1:n.511+15018_511+15019insCACTGCTACTA
NM_001281740.2:c.511+15018_511+15019insCACTGCTACTA	NP_001268669.1:n.511+15018_511+15019insCACTGCTACTA
NM_025135.3:c.511+15018_511+15019insCACTGCTACTA	NP_079411.2:n.511+15018_511+15019insCACTGCTACTA
NM_025135.4:c.511+15018_511+15019insCACTGCTACTA	NP_079411.2:n.511+15018_511+15019insCACTGCTACTA
XM_005258349.1:c.511+15018_511+15019insCACTGCTACTA	XP_005258406.1:n.511+15018_511+15019insCACTGCTACTA
XM_005258352.1:c.511+15018_511+15019insCACTGCTACTA	XP_005258409.1:n.511+15018_511+15019insCACTGCTACTA
XM_005258354.1:c.511+15018_511+15019insCACTGCTACTA	XP_005258411.1:n.511+15018_511+15019insCACTGCTACTA
XM_005258355.1:c.511+15018_511+15019insCACTGCTACTA	XP_005258412.1:n.511+15018_511+15019insCACTGCTACTA
XM_011526189.1:c.511+15018_511+15019insCACTGCTACTA	XP_011524491.1:n.511+15018_511+15019insCACTGCTACTA
XM_011526190.1:c.511+15018_511+15019insCACTGCTACTA	XP_011524492.1:n.511+15018_511+15019insCACTGCTACTA
XM_011526191.1:c.511+15018_511+15019insCACTGCTACTA	XP_011524493.1:n.511+15018_511+15019insCACTGCTACTA
XM_011526192.1:c.511+15018_511+15019insCACTGCTACTA	XP_011524494.1:n.511+15018_511+15019insCACTGCTACTA
XM_011526193.1:c.511+15018_511+15019insCACTGCTACTA	XP_011524495.1:n.511+15018_511+15019insCACTGCTACTA
XM_011526194.1:c.277+15018_277+15019insCACTGCTACTA	XP_011524496.1:n.277+15018_277+15019insCACTGCTACTA
XM_011526195.1:c.511+15018_511+15019insCACTGCTACTA	XP_011524497.1:n.511+15018_511+15019insCACTGCTACTA
XM_011526196.1:c.511+15018_511+15019insCACTGCTACTA	XP_011524498.1:n.511+15018_511+15019insCACTGCTACTA
XM_011526197.1:c.511+15018_511+15019insCACTGCTACTA	XP_011524499.1:n.511+15018_511+15019insCACTGCTACTA
XM_005258355.2:c.511+15018_511+15019insCACTGCTACTA	XP_005258412.1:n.511+15018_511+15019insCACTGCTACTA
XM_011526190.2:c.511+15018_511+15019insCACTGCTACTA	XP_011524492.1:n.511+15018_511+15019insCACTGCTACTA
XM_011526193.3:c.511+15018_511+15019insCACTGCTACTA	XP_011524495.1:n.511+15018_511+15019insCACTGCTACTA
XM_017026006.2:c.511+15018_511+15019insCACTGCTACTA	XP_016881495.1:n.511+15018_511+15019insCACTGCTACTA
XM_017026007.1:c.256+15018_256+15019insCACTGCTACTA	XP_016881496.1:n.256+15018_256+15019insCACTGCTACTA
XM_017026008.1:c.511+15018_511+15019insCACTGCTACTA	XP_016881497.1:n.511+15018_511+15019insCACTGCTACTA
XM_017026009.1:c.511+15018_511+15019insCACTGCTACTA	XP_016881498.1:n.511+15018_511+15019insCACTGCTACTA
XM_017026010.1:c.277+15018_277+15019insCACTGCTACTA	XP_016881499.1:n.277+15018_277+15019insCACTGCTACTA
XM_024451268.1:c.-15+15018_-15+15019insCACTGCTACTA	XP_024307036.1:n.-15+15018_-15+15019insCACTGCTACTA
NM_001281739.3:c.511+15018_511+15019insCACTGCTACTA	NP_001268668.1:n.511+15018_511+15019insCACTGCTACTA
NM_001281740.3:c.511+15018_511+15019insCACTGCTACTA MANE Select	NP_001268669.1:n.511+15018_511+15019insCACTGCTACTA
NM_025135.5:c.511+15018_511+15019insCACTGCTACTA	NP_079411.2:n.511+15018_511+15019insCACTGCTACTA