Canonical Allele Identifier: CA363208646

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.26092924C>T , CM000668.2:g.26092924C>T GRCh38
NC_000006.11:g.26093152C>T , CM000668.1:g.26093152C>T GRCh37
NC_000006.10:g.26201131C>T NCBI36
NG_008720.2:g.10644C>T , LRG_748:g.10644C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000485729.2:c.856C>T (HFE) ENSP00000417534.2:p.His286Tyr
ENST00000707188.1:c.391-1890G>A (H2BC4) ENSP00000516775.1:n.391-1890G>A
ENST00000357618.10:c.856C>T (HFE) MANE Select ENSP00000417404.1:p.His286Tyr
ENST00000309234.10:c.856C>T (HFE) ENSP00000311698.6:p.His286Tyr
ENST00000317896.11:c.580C>T (HFE) ENSP00000313776.7:p.His194Tyr
ENST00000336625.12:c.538C>T (HFE) ENSP00000337819.8:p.His180Tyr
ENST00000349999.8:c.592C>T (HFE) ENSP00000259699.6:p.His198Tyr
ENST00000352392.8:c.77-195C>T (HFE) ENSP00000315936.4:n.77-195C>T
ENST00000353147.9:c.316C>T (HFE) ENSP00000312342.5:p.His106Tyr
ENST00000357618.9:c.856C>T (HFE) ENSP00000417404.1:p.His286Tyr
ENST00000397022.7:c.787C>T (HFE) ENSP00000380217.3:p.His263Tyr
ENST00000461397.5:c.814C>T (HFE) ENSP00000420802.1:p.His272Tyr
ENST00000470149.5:c.847C>T (HFE) ENSP00000419725.1:p.His283Tyr
ENST00000483782.1:n.1187C>T (HFE)
ENST00000486147.1:n.699C>T (HFE)
ENST00000488199.5:c.550C>T (HFE) ENSP00000420559.1:p.His184Tyr
ENST00000629531.1:c.132+30849G>A (H2BC3) ENSP00000486472.1:n.132+30849G>A
NM_000410.3:c.856C>T , LRG_748t1:c.856C>T (HFE) NP_000401.1:p.His286Tyr
NM_001300749.1:c.856C>T (HFE) NP_001287678.1:p.His286Tyr
NM_139003.2:c.538C>T (HFE) NP_620572.1:p.His180Tyr
NM_139004.2:c.580C>T (HFE) NP_620573.1:p.His194Tyr
NM_139006.2:c.814C>T (HFE) NP_620575.1:p.His272Tyr
NM_139007.2:c.592C>T (HFE) NP_620576.1:p.His198Tyr
NM_139008.2:c.550C>T (HFE) NP_620577.1:p.His184Tyr
NM_139009.2:c.787C>T (HFE) NP_620578.1:p.His263Tyr
NM_139010.2:c.316C>T (HFE) NP_620579.1:p.His106Tyr
NM_139011.2:c.77-195C>T (HFE) NP_620580.1:n.77-195C>T
XM_011514543.1:c.856C>T (HFE) XP_011512845.1:p.His286Tyr
XM_011514544.1:c.847C>T (HFE) XP_011512846.1:p.His283Tyr
XR_241893.2:n.978C>T (HFE)
XM_011514543.3:c.856C>T (HFE) XP_011512845.1:p.His286Tyr
XR_241893.4:n.950C>T (HFE)
NM_001300749.2:c.856C>T (HFE) NP_001287678.1:p.His286Tyr
NM_139003.3:c.538C>T (HFE) NP_620572.1:p.His180Tyr
NM_139004.3:c.580C>T (HFE) NP_620573.1:p.His194Tyr
NM_139006.3:c.814C>T (HFE) NP_620575.1:p.His272Tyr
NM_139007.3:c.592C>T (HFE) NP_620576.1:p.His198Tyr
NM_139008.3:c.550C>T (HFE) NP_620577.1:p.His184Tyr
NM_139009.3:c.787C>T (HFE) NP_620578.1:p.His263Tyr
NM_139010.3:c.316C>T (HFE) NP_620579.1:p.His106Tyr
NM_139011.3:c.77-195C>T (HFE) NP_620580.1:n.77-195C>T
NM_000410.4:c.856C>T (HFE) MANE Select NP_000401.1:p.His286Tyr
NM_001384164.1:c.856C>T (HFE) NP_001371093.1:p.His286Tyr