Canonical Allele Identifier: CA1616889874

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.26092733C= , CM000668.2:g.26092733C= GRCh38
NC_000006.11:g.26092961C= , CM000668.1:g.26092961C= GRCh37
NC_000006.10:g.26200940C= NCBI36
NG_008720.2:g.10453C= , LRG_748:g.10453C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000485729.2:c.665C= (HFE) ENSP00000417534.2:p.Thr222=
ENST00000707188.1:c.391-1699G= (H2BC4) ENSP00000516775.1:n.391-1699G=
ENST00000357618.10:c.665C= (HFE) MANE Select ENSP00000417404.1:p.Thr222=
ENST00000309234.10:c.665C= (HFE) ENSP00000311698.6:p.Thr222=
ENST00000317896.11:c.389C= (HFE) ENSP00000313776.7:p.Thr130=
ENST00000336625.12:c.347C= (HFE) ENSP00000337819.8:p.Thr116=
ENST00000349999.8:c.401C= (HFE) ENSP00000259699.6:p.Thr134=
ENST00000352392.8:c.77-386C= (HFE) ENSP00000315936.4:n.77-386C=
ENST00000353147.9:c.125C= (HFE) ENSP00000312342.5:p.Thr42=
ENST00000357618.9:c.665C= (HFE) ENSP00000417404.1:p.Thr222=
ENST00000397022.7:c.596C= (HFE) ENSP00000380217.3:p.Thr199=
ENST00000461397.5:c.623C= (HFE) ENSP00000420802.1:p.Thr208=
ENST00000470149.5:c.656C= (HFE) ENSP00000419725.1:p.Thr219=
ENST00000483782.1:n.996C= (HFE)
ENST00000486147.1:n.508C= (HFE)
ENST00000488199.5:c.359C= (HFE) ENSP00000420559.1:p.Thr120=
ENST00000629531.1:c.132+31040G= (H2BC3) ENSP00000486472.1:n.132+31040G=
NM_000410.3:c.665C= , LRG_748t1:c.665C= (HFE) NP_000401.1:p.Thr222=
NM_001300749.1:c.665C= (HFE) NP_001287678.1:p.Thr222=
NM_139003.2:c.347C= (HFE) NP_620572.1:p.Thr116=
NM_139004.2:c.389C= (HFE) NP_620573.1:p.Thr130=
NM_139006.2:c.623C= (HFE) NP_620575.1:p.Thr208=
NM_139007.2:c.401C= (HFE) NP_620576.1:p.Thr134=
NM_139008.2:c.359C= (HFE) NP_620577.1:p.Thr120=
NM_139009.2:c.596C= (HFE) NP_620578.1:p.Thr199=
NM_139010.2:c.125C= (HFE) NP_620579.1:p.Thr42=
NM_139011.2:c.77-386C= (HFE) NP_620580.1:n.77-386C=
XM_011514543.1:c.665C= (HFE) XP_011512845.1:p.Thr222=
XM_011514544.1:c.656C= (HFE) XP_011512846.1:p.Thr219=
XR_241893.2:n.787C= (HFE)
XM_011514543.3:c.665C= (HFE) XP_011512845.1:p.Thr222=
XR_241893.4:n.759C= (HFE)
NM_001300749.2:c.665C= (HFE) NP_001287678.1:p.Thr222=
NM_139003.3:c.347C= (HFE) NP_620572.1:p.Thr116=
NM_139004.3:c.389C= (HFE) NP_620573.1:p.Thr130=
NM_139006.3:c.623C= (HFE) NP_620575.1:p.Thr208=
NM_139007.3:c.401C= (HFE) NP_620576.1:p.Thr134=
NM_139008.3:c.359C= (HFE) NP_620577.1:p.Thr120=
NM_139009.3:c.596C= (HFE) NP_620578.1:p.Thr199=
NM_139010.3:c.125C= (HFE) NP_620579.1:p.Thr42=
NM_139011.3:c.77-386C= (HFE) NP_620580.1:n.77-386C=
NM_000410.4:c.665C= (HFE) MANE Select NP_000401.1:p.Thr222=
NM_001384164.1:c.665C= (HFE) NP_001371093.1:p.Thr222=