Canonical Allele Identifier: CA363208474

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.26092899G>T , CM000668.2:g.26092899G>T GRCh38
NC_000006.11:g.26093127G>T , CM000668.1:g.26093127G>T GRCh37
NC_000006.10:g.26201106G>T NCBI36
NG_008720.2:g.10619G>T , LRG_748:g.10619G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000485729.2:c.831G>T (HFE) ENSP00000417534.2:p.Glu277Asp
ENST00000707188.1:c.391-1865C>A (H2BC4) ENSP00000516775.1:n.391-1865C>A
ENST00000357618.10:c.831G>T (HFE) MANE Select ENSP00000417404.1:p.Glu277Asp
ENST00000309234.10:c.831G>T (HFE) ENSP00000311698.6:p.Glu277Asp
ENST00000317896.11:c.555G>T (HFE) ENSP00000313776.7:p.Glu185Asp
ENST00000336625.12:c.513G>T (HFE) ENSP00000337819.8:p.Glu171Asp
ENST00000349999.8:c.567G>T (HFE) ENSP00000259699.6:p.Glu189Asp
ENST00000352392.8:c.77-220G>T (HFE) ENSP00000315936.4:n.77-220G>T
ENST00000353147.9:c.291G>T (HFE) ENSP00000312342.5:p.Glu97Asp
ENST00000357618.9:c.831G>T (HFE) ENSP00000417404.1:p.Glu277Asp
ENST00000397022.7:c.762G>T (HFE) ENSP00000380217.3:p.Glu254Asp
ENST00000461397.5:c.789G>T (HFE) ENSP00000420802.1:p.Glu263Asp
ENST00000470149.5:c.822G>T (HFE) ENSP00000419725.1:p.Glu274Asp
ENST00000483782.1:n.1162G>T (HFE)
ENST00000486147.1:n.674G>T (HFE)
ENST00000488199.5:c.525G>T (HFE) ENSP00000420559.1:p.Glu175Asp
ENST00000629531.1:c.132+30874C>A (H2BC3) ENSP00000486472.1:n.132+30874C>A
NM_000410.3:c.831G>T , LRG_748t1:c.831G>T (HFE) NP_000401.1:p.Glu277Asp
NM_001300749.1:c.831G>T (HFE) NP_001287678.1:p.Glu277Asp
NM_139003.2:c.513G>T (HFE) NP_620572.1:p.Glu171Asp
NM_139004.2:c.555G>T (HFE) NP_620573.1:p.Glu185Asp
NM_139006.2:c.789G>T (HFE) NP_620575.1:p.Glu263Asp
NM_139007.2:c.567G>T (HFE) NP_620576.1:p.Glu189Asp
NM_139008.2:c.525G>T (HFE) NP_620577.1:p.Glu175Asp
NM_139009.2:c.762G>T (HFE) NP_620578.1:p.Glu254Asp
NM_139010.2:c.291G>T (HFE) NP_620579.1:p.Glu97Asp
NM_139011.2:c.77-220G>T (HFE) NP_620580.1:n.77-220G>T
XM_011514543.1:c.831G>T (HFE) XP_011512845.1:p.Glu277Asp
XM_011514544.1:c.822G>T (HFE) XP_011512846.1:p.Glu274Asp
XR_241893.2:n.953G>T (HFE)
XM_011514543.3:c.831G>T (HFE) XP_011512845.1:p.Glu277Asp
XR_241893.4:n.925G>T (HFE)
NM_001300749.2:c.831G>T (HFE) NP_001287678.1:p.Glu277Asp
NM_139003.3:c.513G>T (HFE) NP_620572.1:p.Glu171Asp
NM_139004.3:c.555G>T (HFE) NP_620573.1:p.Glu185Asp
NM_139006.3:c.789G>T (HFE) NP_620575.1:p.Glu263Asp
NM_139007.3:c.567G>T (HFE) NP_620576.1:p.Glu189Asp
NM_139008.3:c.525G>T (HFE) NP_620577.1:p.Glu175Asp
NM_139009.3:c.762G>T (HFE) NP_620578.1:p.Glu254Asp
NM_139010.3:c.291G>T (HFE) NP_620579.1:p.Glu97Asp
NM_139011.3:c.77-220G>T (HFE) NP_620580.1:n.77-220G>T
NM_000410.4:c.831G>T (HFE) MANE Select NP_000401.1:p.Glu277Asp
NM_001384164.1:c.831G>T (HFE) NP_001371093.1:p.Glu277Asp