Canonical Allele Identifier: CA8942237

Gene: FHOD3

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.36744128G>A , CM000680.2:g.36744128G>A	GRCh38
NC_000018.9:g.34324091G>A , CM000680.1:g.34324091G>A	GRCh37
NC_000018.8:g.32578089G>A	NCBI36
NG_042837.1:g.451433G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000590592.6:c.3976G>A MANE Select	ENSP00000466937.1:p.Val1326Ile
ENST00000257209.8:c.3451G>A	ENSP00000257209.3:p.Val1151Ile
ENST00000359247.8:c.3400G>A	ENSP00000352186.3:p.Val1134Ile
ENST00000585579.2:c.501G>A
ENST00000590592.5:c.3976G>A	ENSP00000466937.1:p.Val1326Ile
ENST00000591635.5:c.1039G>A	ENSP00000467195.1:p.Val347Ile
ENST00000592128.5:c.718G>A	ENSP00000467462.2:p.Val240Ile
ENST00000592930.5:c.2732G>A
NM_001281739.1:c.3400G>A	NP_001268668.1:p.Val1134Ile
NM_001281739.2:c.3400G>A	NP_001268668.1:p.Val1134Ile
NM_001281740.1:c.3976G>A	NP_001268669.1:p.Val1326Ile
NM_001281740.2:c.3976G>A	NP_001268669.1:p.Val1326Ile
NM_025135.3:c.3451G>A	NP_079411.2:p.Val1151Ile
NM_025135.4:c.3451G>A	NP_079411.2:p.Val1151Ile
XM_005258349.1:c.3787G>A	XP_005258406.1:p.Val1263Ile
XM_005258352.1:c.3400G>A	XP_005258409.1:p.Val1134Ile
XM_005258354.1:c.3337G>A	XP_005258411.1:p.Val1113Ile
XM_005258355.1:c.3337G>A	XP_005258412.1:p.Val1113Ile
XM_011526189.1:c.4036G>A	XP_011524491.1:p.Val1346Ile
XM_011526190.1:c.4036G>A	XP_011524492.1:p.Val1346Ile
XM_011526191.1:c.3985G>A	XP_011524493.1:p.Val1329Ile
XM_011526192.1:c.3961G>A	XP_011524494.1:p.Val1321Ile
XM_011526193.1:c.4036G>A	XP_011524495.1:p.Val1346Ile
XM_011526194.1:c.3802G>A	XP_011524496.1:p.Val1268Ile
XM_011526195.1:c.3739G>A	XP_011524497.1:p.Val1247Ile
XM_011526196.1:c.3511G>A	XP_011524498.1:p.Val1171Ile
XM_011526197.1:c.3961G>A	XP_011524499.1:p.Val1321Ile
XM_005258355.2:c.3337G>A	XP_005258412.1:p.Val1113Ile
XM_011526190.2:c.4036G>A	XP_011524492.1:p.Val1346Ile
XM_011526193.3:c.4036G>A	XP_011524495.1:p.Val1346Ile
XM_017026006.2:c.4036G>A	XP_016881495.1:p.Val1346Ile
XM_017026007.1:c.3781G>A	XP_016881496.1:p.Val1261Ile
XM_017026008.1:c.4036G>A	XP_016881497.1:p.Val1346Ile
XM_017026009.1:c.3451G>A	XP_016881498.1:p.Val1151Ile
XM_017026010.1:c.3802G>A	XP_016881499.1:p.Val1268Ile
XM_024451268.1:c.3511G>A	XP_024307036.1:p.Val1171Ile
NM_001281739.3:c.3400G>A	NP_001268668.1:p.Val1134Ile
NM_001281740.3:c.3976G>A MANE Select	NP_001268669.1:p.Val1326Ile
NM_025135.5:c.3451G>A	NP_079411.2:p.Val1151Ile