Canonical Allele Identifier: CA2296194107

Gene: FHOD3

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.36672723T= , CM000680.2:g.36672723T=	GRCh38
NC_000018.9:g.34252686T= , CM000680.1:g.34252686T=	GRCh37
NC_000018.8:g.32506684T=	NCBI36
NG_042837.1:g.380028T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000590592.6:c.1836-8713T= MANE Select	ENSP00000466937.1:n.1836-8713T=
ENST00000257209.8:c.1311-8713T=	ENSP00000257209.3:n.1311-8713T=
ENST00000359247.8:c.1311-8713T=	ENSP00000352186.3:n.1311-8713T=
ENST00000589114.5:n.1430-8713T=
ENST00000590592.5:c.1836-8713T=	ENSP00000466937.1:n.1836-8713T=
ENST00000591635.5:c.276+14593T=	ENSP00000467195.1:n.276+14593T=
ENST00000592930.5:c.592-8713T=
NM_001281739.1:c.1311-8713T=	NP_001268668.1:n.1311-8713T=
NM_001281739.2:c.1311-8713T=	NP_001268668.1:n.1311-8713T=
NM_001281740.1:c.1836-8713T=	NP_001268669.1:n.1836-8713T=
NM_001281740.2:c.1836-8713T=	NP_001268669.1:n.1836-8713T=
NM_025135.3:c.1311-8713T=	NP_079411.2:n.1311-8713T=
NM_025135.4:c.1311-8713T=	NP_079411.2:n.1311-8713T=
XM_005258349.1:c.1647-8713T=	XP_005258406.1:n.1647-8713T=
XM_005258352.1:c.1311-8713T=	XP_005258409.1:n.1311-8713T=
XM_005258354.1:c.1197-8713T=	XP_005258411.1:n.1197-8713T=
XM_005258355.1:c.1197-8713T=	XP_005258412.1:n.1197-8713T=
XM_011526189.1:c.1836-8550T=	XP_011524491.1:n.1836-8550T=
XM_011526190.1:c.1836-8550T=	XP_011524492.1:n.1836-8550T=
XM_011526191.1:c.1836-8550T=	XP_011524493.1:n.1836-8550T=
XM_011526192.1:c.1761-8550T=	XP_011524494.1:n.1761-8550T=
XM_011526193.1:c.1836-8550T=	XP_011524495.1:n.1836-8550T=
XM_011526194.1:c.1602-8550T=	XP_011524496.1:n.1602-8550T=
XM_011526195.1:c.1836-8550T=	XP_011524497.1:n.1836-8550T=
XM_011526196.1:c.1311-8550T=	XP_011524498.1:n.1311-8550T=
XM_011526197.1:c.1761-8550T=	XP_011524499.1:n.1761-8550T=
XM_005258355.2:c.1197-8713T=	XP_005258412.1:n.1197-8713T=
XM_011526190.2:c.1836-8550T=	XP_011524492.1:n.1836-8550T=
XM_011526193.3:c.1836-8550T=	XP_011524495.1:n.1836-8550T=
XM_017026006.2:c.1836-8550T=	XP_016881495.1:n.1836-8550T=
XM_017026007.1:c.1581-8550T=	XP_016881496.1:n.1581-8550T=
XM_017026008.1:c.1836-8550T=	XP_016881497.1:n.1836-8550T=
XM_017026009.1:c.1311-8713T=	XP_016881498.1:n.1311-8713T=
XM_017026010.1:c.1602-8550T=	XP_016881499.1:n.1602-8550T=
XM_024451268.1:c.1311-8550T=	XP_024307036.1:n.1311-8550T=
NM_001281739.3:c.1311-8713T=	NP_001268668.1:n.1311-8713T=
NM_001281740.3:c.1836-8713T= MANE Select	NP_001268669.1:n.1836-8713T=
NM_025135.5:c.1311-8713T=	NP_079411.2:n.1311-8713T=