Canonical Allele Identifier: CA136294453
Community Standard Title: NM_000410.4(HFE):c.*281C>T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.26094507C>T , CM000668.2:g.26094507C>T GRCh38
NC_000006.11:g.26094735C>T , CM000668.1:g.26094735C>T GRCh37
NC_000006.10:g.26202714C>T NCBI36
NG_008720.2:g.12227C>T , LRG_748:g.12227C>T

Transcript Alleles

HGVS Amino-acid Change
NM_000410.4:c.*281C>T (HFE) MANE Select NP_000401.1:n.*281C>T
ENST00000357618.10:c.*281C>T (HFE) MANE Select ENSP00000417404.1:n.*281C>T
NM_000410.3:c.*281C>T , LRG_748t1:c.*281C>T (HFE) NP_000401.1:n.*281C>T
NM_001300749.1:c.*96C>T (HFE) NP_001287678.1:n.*96C>T
NM_001300749.2:c.*96C>T (HFE) NP_001287678.1:n.*96C>T
NM_001384164.1:c.*96C>T (HFE) NP_001371093.1:n.*96C>T
NM_139003.2:c.*281C>T (HFE) NP_620572.1:n.*281C>T
NM_139003.3:c.*281C>T (HFE) NP_620572.1:n.*281C>T
NM_139004.2:c.*281C>T (HFE) NP_620573.1:n.*281C>T
NM_139004.3:c.*281C>T (HFE) NP_620573.1:n.*281C>T
NM_139006.2:c.*281C>T (HFE) NP_620575.1:n.*281C>T
NM_139006.3:c.*281C>T (HFE) NP_620575.1:n.*281C>T
NM_139007.2:c.*281C>T (HFE) NP_620576.1:n.*281C>T
NM_139007.3:c.*281C>T (HFE) NP_620576.1:n.*281C>T
NM_139008.2:c.*281C>T (HFE) NP_620577.1:n.*281C>T
NM_139008.3:c.*281C>T (HFE) NP_620577.1:n.*281C>T
NM_139009.2:c.*281C>T (HFE) NP_620578.1:n.*281C>T
NM_139009.3:c.*281C>T (HFE) NP_620578.1:n.*281C>T
NM_139010.2:c.*281C>T (HFE) NP_620579.1:n.*281C>T
NM_139010.3:c.*281C>T (HFE) NP_620579.1:n.*281C>T
NM_139011.2:c.*281C>T (HFE) NP_620580.1:n.*281C>T
NM_139011.3:c.*281C>T (HFE) NP_620580.1:n.*281C>T
ENST00000309234.10:c.*96C>T (HFE) ENSP00000311698.6:n.*96C>T
ENST00000317896.11:c.*281C>T (HFE) ENSP00000313776.7:n.*281C>T
ENST00000349999.8:c.*281C>T (HFE) ENSP00000259699.6:n.*281C>T
ENST00000357618.9:c.*281C>T (HFE) ENSP00000417404.1:n.*281C>T
ENST00000485729.1:c.264C>T (HFE) ENSP00000417534.1:n.264C>T
ENST00000485729.2:c.*96C>T (HFE) ENSP00000417534.2:n.*96C>T
ENST00000629531.1:c.132+29266G>A (H2BC3) ENSP00000486472.1:n.132+29266G>A
ENST00000707188.1:c.391-3473G>A (H2BC4) ENSP00000516775.1:n.391-3473G>A
XM_011514543.1:c.*96C>T (HFE) XP_011512845.1:n.*96C>T
XM_011514543.3:c.*96C>T (HFE) XP_011512845.1:n.*96C>T
XM_011514544.1:c.*281C>T (HFE) XP_011512846.1:n.*281C>T