Canonical Allele Identifier: CA2296131283

Gene: FHOD3

Linked Data

• dbSNP Id: rs2057005024

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.36536616_36536617insG , CM000680.2:g.36536616_36536617insG	GRCh38
NC_000018.9:g.34116579_34116580insG , CM000680.1:g.34116579_34116580insG	GRCh37
NC_000018.8:g.32370577_32370578insG	NCBI36
NG_042837.1:g.243921_243922insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000590592.6:c.511+24073_511+24074insG MANE Select	ENSP00000466937.1:n.511+24073_511+24074insG
ENST00000257209.8:c.511+24073_511+24074insG	ENSP00000257209.3:n.511+24073_511+24074insG
ENST00000359247.8:c.511+24073_511+24074insG	ENSP00000352186.3:n.511+24073_511+24074insG
ENST00000589114.5:n.630+24073_630+24074insG
ENST00000590592.5:c.511+24073_511+24074insG	ENSP00000466937.1:n.511+24073_511+24074insG
NM_001281739.1:c.511+24073_511+24074insG	NP_001268668.1:n.511+24073_511+24074insG
NM_001281739.2:c.511+24073_511+24074insG	NP_001268668.1:n.511+24073_511+24074insG
NM_001281740.1:c.511+24073_511+24074insG	NP_001268669.1:n.511+24073_511+24074insG
NM_001281740.2:c.511+24073_511+24074insG	NP_001268669.1:n.511+24073_511+24074insG
NM_025135.3:c.511+24073_511+24074insG	NP_079411.2:n.511+24073_511+24074insG
NM_025135.4:c.511+24073_511+24074insG	NP_079411.2:n.511+24073_511+24074insG
XM_005258349.1:c.511+24073_511+24074insG	XP_005258406.1:n.511+24073_511+24074insG
XM_005258352.1:c.511+24073_511+24074insG	XP_005258409.1:n.511+24073_511+24074insG
XM_005258354.1:c.511+24073_511+24074insG	XP_005258411.1:n.511+24073_511+24074insG
XM_005258355.1:c.511+24073_511+24074insG	XP_005258412.1:n.511+24073_511+24074insG
XM_011526189.1:c.511+24073_511+24074insG	XP_011524491.1:n.511+24073_511+24074insG
XM_011526190.1:c.511+24073_511+24074insG	XP_011524492.1:n.511+24073_511+24074insG
XM_011526191.1:c.511+24073_511+24074insG	XP_011524493.1:n.511+24073_511+24074insG
XM_011526192.1:c.511+24073_511+24074insG	XP_011524494.1:n.511+24073_511+24074insG
XM_011526193.1:c.511+24073_511+24074insG	XP_011524495.1:n.511+24073_511+24074insG
XM_011526194.1:c.277+24073_277+24074insG	XP_011524496.1:n.277+24073_277+24074insG
XM_011526195.1:c.511+24073_511+24074insG	XP_011524497.1:n.511+24073_511+24074insG
XM_011526196.1:c.511+24073_511+24074insG	XP_011524498.1:n.511+24073_511+24074insG
XM_011526197.1:c.511+24073_511+24074insG	XP_011524499.1:n.511+24073_511+24074insG
XM_005258355.2:c.511+24073_511+24074insG	XP_005258412.1:n.511+24073_511+24074insG
XM_011526190.2:c.511+24073_511+24074insG	XP_011524492.1:n.511+24073_511+24074insG
XM_011526193.3:c.511+24073_511+24074insG	XP_011524495.1:n.511+24073_511+24074insG
XM_017026006.2:c.511+24073_511+24074insG	XP_016881495.1:n.511+24073_511+24074insG
XM_017026007.1:c.256+24073_256+24074insG	XP_016881496.1:n.256+24073_256+24074insG
XM_017026008.1:c.511+24073_511+24074insG	XP_016881497.1:n.511+24073_511+24074insG
XM_017026009.1:c.511+24073_511+24074insG	XP_016881498.1:n.511+24073_511+24074insG
XM_017026010.1:c.277+24073_277+24074insG	XP_016881499.1:n.277+24073_277+24074insG
XM_024451268.1:c.-15+24073_-15+24074insG	XP_024307036.1:n.-15+24073_-15+24074insG
NM_001281739.3:c.511+24073_511+24074insG	NP_001268668.1:n.511+24073_511+24074insG
NM_001281740.3:c.511+24073_511+24074insG MANE Select	NP_001268669.1:n.511+24073_511+24074insG
NM_025135.5:c.511+24073_511+24074insG	NP_079411.2:n.511+24073_511+24074insG