Canonical Allele Identifier: CA1616889954

Gene: HFE H2BC4 H2BC3

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.26092911G= , CM000668.2:g.26092911G=	GRCh38
NC_000006.11:g.26093139G= , CM000668.1:g.26093139G=	GRCh37
NC_000006.10:g.26201118G=	NCBI36
NG_008720.2:g.10631G= , LRG_748:g.10631G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000485729.2:c.843G= (HFE)	ENSP00000417534.2:p.Thr281=
ENST00000707188.1:c.391-1877C= (H2BC4)	ENSP00000516775.1:n.391-1877C=
ENST00000357618.10:c.843G= (HFE) MANE Select	ENSP00000417404.1:p.Thr281=
ENST00000309234.10:c.843G= (HFE)	ENSP00000311698.6:p.Thr281=
ENST00000317896.11:c.567G= (HFE)	ENSP00000313776.7:p.Thr189=
ENST00000336625.12:c.525G= (HFE)	ENSP00000337819.8:p.Thr175=
ENST00000349999.8:c.579G= (HFE)	ENSP00000259699.6:p.Thr193=
ENST00000352392.8:c.77-208G= (HFE)	ENSP00000315936.4:n.77-208G=
ENST00000353147.9:c.303G= (HFE)	ENSP00000312342.5:p.Thr101=
ENST00000357618.9:c.843G= (HFE)	ENSP00000417404.1:p.Thr281=
ENST00000397022.7:c.774G= (HFE)	ENSP00000380217.3:p.Thr258=
ENST00000461397.5:c.801G= (HFE)	ENSP00000420802.1:p.Thr267=
ENST00000470149.5:c.834G= (HFE)	ENSP00000419725.1:p.Thr278=
ENST00000483782.1:n.1174G= (HFE)
ENST00000486147.1:n.686G= (HFE)
ENST00000488199.5:c.537G= (HFE)	ENSP00000420559.1:p.Thr179=
ENST00000629531.1:c.132+30862C= (H2BC3)	ENSP00000486472.1:n.132+30862C=
NM_000410.3:c.843G= , LRG_748t1:c.843G= (HFE)	NP_000401.1:p.Thr281=
NM_001300749.1:c.843G= (HFE)	NP_001287678.1:p.Thr281=
NM_139003.2:c.525G= (HFE)	NP_620572.1:p.Thr175=
NM_139004.2:c.567G= (HFE)	NP_620573.1:p.Thr189=
NM_139006.2:c.801G= (HFE)	NP_620575.1:p.Thr267=
NM_139007.2:c.579G= (HFE)	NP_620576.1:p.Thr193=
NM_139008.2:c.537G= (HFE)	NP_620577.1:p.Thr179=
NM_139009.2:c.774G= (HFE)	NP_620578.1:p.Thr258=
NM_139010.2:c.303G= (HFE)	NP_620579.1:p.Thr101=
NM_139011.2:c.77-208G= (HFE)	NP_620580.1:n.77-208G=
XM_011514543.1:c.843G= (HFE)	XP_011512845.1:p.Thr281=
XM_011514544.1:c.834G= (HFE)	XP_011512846.1:p.Thr278=
XR_241893.2:n.965G= (HFE)
XM_011514543.3:c.843G= (HFE)	XP_011512845.1:p.Thr281=
XR_241893.4:n.937G= (HFE)
NM_001300749.2:c.843G= (HFE)	NP_001287678.1:p.Thr281=
NM_139003.3:c.525G= (HFE)	NP_620572.1:p.Thr175=
NM_139004.3:c.567G= (HFE)	NP_620573.1:p.Thr189=
NM_139006.3:c.801G= (HFE)	NP_620575.1:p.Thr267=
NM_139007.3:c.579G= (HFE)	NP_620576.1:p.Thr193=
NM_139008.3:c.537G= (HFE)	NP_620577.1:p.Thr179=
NM_139009.3:c.774G= (HFE)	NP_620578.1:p.Thr258=
NM_139010.3:c.303G= (HFE)	NP_620579.1:p.Thr101=
NM_139011.3:c.77-208G= (HFE)	NP_620580.1:n.77-208G=
NM_000410.4:c.843G= (HFE) MANE Select	NP_000401.1:p.Thr281=
NM_001384164.1:c.843G= (HFE)	NP_001371093.1:p.Thr281=