Canonical Allele Identifier: CA1616889919

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.26092833C= , CM000668.2:g.26092833C= GRCh38
NC_000006.11:g.26093061C= , CM000668.1:g.26093061C= GRCh37
NC_000006.10:g.26201040C= NCBI36
NG_008720.2:g.10553C= , LRG_748:g.10553C=

Transcript Alleles

HGVS Amino-acid change
ENST00000485729.2:c.765C= (HFE) ENSP00000417534.2:p.Asp255=
ENST00000707188.1:c.391-1799G= (H2BC4) ENSP00000516775.1:n.391-1799G=
ENST00000357618.10:c.765C= (HFE) MANE Select ENSP00000417404.1:p.Asp255=
ENST00000309234.10:c.765C= (HFE) ENSP00000311698.6:p.Asp255=
ENST00000317896.11:c.489C= (HFE) ENSP00000313776.7:p.Asp163=
ENST00000336625.12:c.447C= (HFE) ENSP00000337819.8:p.Asp149=
ENST00000349999.8:c.501C= (HFE) ENSP00000259699.6:p.Asp167=
ENST00000352392.8:c.77-286C= (HFE) ENSP00000315936.4:n.77-286C=
ENST00000353147.9:c.225C= (HFE) ENSP00000312342.5:p.Asp75=
ENST00000357618.9:c.765C= (HFE) ENSP00000417404.1:p.Asp255=
ENST00000397022.7:c.696C= (HFE) ENSP00000380217.3:p.Asp232=
ENST00000461397.5:c.723C= (HFE) ENSP00000420802.1:p.Asp241=
ENST00000470149.5:c.756C= (HFE) ENSP00000419725.1:p.Asp252=
ENST00000483782.1:n.1096C= (HFE)
ENST00000486147.1:n.608C= (HFE)
ENST00000488199.5:c.459C= (HFE) ENSP00000420559.1:p.Asp153=
ENST00000629531.1:c.132+30940G= (H2BC3) ENSP00000486472.1:n.132+30940G=
NM_000410.3:c.765C= , LRG_748t1:c.765C= (HFE) NP_000401.1:p.Asp255=
NM_001300749.1:c.765C= (HFE) NP_001287678.1:p.Asp255=
NM_139003.2:c.447C= (HFE) NP_620572.1:p.Asp149=
NM_139004.2:c.489C= (HFE) NP_620573.1:p.Asp163=
NM_139006.2:c.723C= (HFE) NP_620575.1:p.Asp241=
NM_139007.2:c.501C= (HFE) NP_620576.1:p.Asp167=
NM_139008.2:c.459C= (HFE) NP_620577.1:p.Asp153=
NM_139009.2:c.696C= (HFE) NP_620578.1:p.Asp232=
NM_139010.2:c.225C= (HFE) NP_620579.1:p.Asp75=
NM_139011.2:c.77-286C= (HFE) NP_620580.1:n.77-286C=
XM_011514543.1:c.765C= (HFE) XP_011512845.1:p.Asp255=
XM_011514544.1:c.756C= (HFE) XP_011512846.1:p.Asp252=
XR_241893.2:n.887C= (HFE)
XM_011514543.3:c.765C= (HFE) XP_011512845.1:p.Asp255=
XR_241893.4:n.859C= (HFE)
NM_001300749.2:c.765C= (HFE) NP_001287678.1:p.Asp255=
NM_139003.3:c.447C= (HFE) NP_620572.1:p.Asp149=
NM_139004.3:c.489C= (HFE) NP_620573.1:p.Asp163=
NM_139006.3:c.723C= (HFE) NP_620575.1:p.Asp241=
NM_139007.3:c.501C= (HFE) NP_620576.1:p.Asp167=
NM_139008.3:c.459C= (HFE) NP_620577.1:p.Asp153=
NM_139009.3:c.696C= (HFE) NP_620578.1:p.Asp232=
NM_139010.3:c.225C= (HFE) NP_620579.1:p.Asp75=
NM_139011.3:c.77-286C= (HFE) NP_620580.1:n.77-286C=
NM_000410.4:c.765C= (HFE) MANE Select NP_000401.1:p.Asp255=
NM_001384164.1:c.765C= (HFE) NP_001371093.1:p.Asp255=