Canonical Allele Identifier: CA2578549132

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.26092657del , CM000668.2:g.26092657del GRCh38
NC_000006.11:g.26092885del , CM000668.1:g.26092885del GRCh37
NC_000006.10:g.26200864del NCBI36
NG_008720.2:g.10377del , LRG_748:g.10377del

Transcript Alleles

HGVS Amino-acid Change
ENST00000485729.2:c.617-28del (HFE) ENSP00000417534.2:n.617-28del
ENST00000707188.1:c.391-1623del (H2BC4) ENSP00000516775.1:n.391-1623del
ENST00000357618.10:c.617-28del (HFE) MANE Select ENSP00000417404.1:n.617-28del
ENST00000309234.10:c.617-28del (HFE) ENSP00000311698.6:n.617-28del
ENST00000317896.11:c.341-28del (HFE) ENSP00000313776.7:n.341-28del
ENST00000336625.12:c.341-70del (HFE) ENSP00000337819.8:n.341-70del
ENST00000349999.8:c.353-28del (HFE) ENSP00000259699.6:n.353-28del
ENST00000352392.8:c.77-462del (HFE) ENSP00000315936.4:n.77-462del
ENST00000353147.9:c.77-28del (HFE) ENSP00000312342.5:n.77-28del
ENST00000357618.9:c.617-28del (HFE) ENSP00000417404.1:n.617-28del
ENST00000397022.7:c.548-28del (HFE) ENSP00000380217.3:n.548-28del
ENST00000461397.5:c.617-70del (HFE) ENSP00000420802.1:n.617-70del
ENST00000470149.5:c.649+16del (HFE) ENSP00000419725.1:n.649+16del
ENST00000483782.1:n.948-28del (HFE)
ENST00000486147.1:n.432del (HFE)
ENST00000488199.5:c.353-70del (HFE) ENSP00000420559.1:n.353-70del
ENST00000629531.1:c.132+31116del (H2BC3) ENSP00000486472.1:n.132+31116del
NM_000410.3:c.617-28del , LRG_748t1:c.617-28del (HFE) NP_000401.1:n.617-28del
NM_001300749.1:c.617-28del (HFE) NP_001287678.1:n.617-28del
NM_139003.2:c.341-70del (HFE) NP_620572.1:n.341-70del
NM_139004.2:c.341-28del (HFE) NP_620573.1:n.341-28del
NM_139006.2:c.617-70del (HFE) NP_620575.1:n.617-70del
NM_139007.2:c.353-28del (HFE) NP_620576.1:n.353-28del
NM_139008.2:c.353-70del (HFE) NP_620577.1:n.353-70del
NM_139009.2:c.548-28del (HFE) NP_620578.1:n.548-28del
NM_139010.2:c.77-28del (HFE) NP_620579.1:n.77-28del
NM_139011.2:c.77-462del (HFE) NP_620580.1:n.77-462del
XM_011514543.1:c.617-28del (HFE) XP_011512845.1:n.617-28del
XM_011514544.1:c.649+16del (HFE) XP_011512846.1:n.649+16del
XR_241893.2:n.739-28del (HFE)
XM_011514543.3:c.617-28del (HFE) XP_011512845.1:n.617-28del
XR_241893.4:n.711-28del (HFE)
NM_001300749.2:c.617-28del (HFE) NP_001287678.1:n.617-28del
NM_139003.3:c.341-70del (HFE) NP_620572.1:n.341-70del
NM_139004.3:c.341-28del (HFE) NP_620573.1:n.341-28del
NM_139006.3:c.617-70del (HFE) NP_620575.1:n.617-70del
NM_139007.3:c.353-28del (HFE) NP_620576.1:n.353-28del
NM_139008.3:c.353-70del (HFE) NP_620577.1:n.353-70del
NM_139009.3:c.548-28del (HFE) NP_620578.1:n.548-28del
NM_139010.3:c.77-28del (HFE) NP_620579.1:n.77-28del
NM_139011.3:c.77-462del (HFE) NP_620580.1:n.77-462del
NM_000410.4:c.617-28del (HFE) MANE Select NP_000401.1:n.617-28del
NM_001384164.1:c.617-28del (HFE) NP_001371093.1:n.617-28del