Canonical Allele Identifier: CA1616889976

Gene: HFE H2BC4 H2BC3

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.26092952T= , CM000668.2:g.26092952T=	GRCh38
NC_000006.11:g.26093180T= , CM000668.1:g.26093180T=	GRCh37
NC_000006.10:g.26201159T=	NCBI36
NG_008720.2:g.10672T= , LRG_748:g.10672T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000485729.2:c.884T= (HFE)	ENSP00000417534.2:p.Val295=
ENST00000707188.1:c.391-1918A= (H2BC4)	ENSP00000516775.1:n.391-1918A=
ENST00000357618.10:c.884T= (HFE) MANE Select	ENSP00000417404.1:p.Val295=
ENST00000309234.10:c.884T= (HFE)	ENSP00000311698.6:p.Val295=
ENST00000317896.11:c.608T= (HFE)	ENSP00000313776.7:p.Val203=
ENST00000336625.12:c.566T= (HFE)	ENSP00000337819.8:p.Val189=
ENST00000349999.8:c.620T= (HFE)	ENSP00000259699.6:p.Val207=
ENST00000352392.8:c.77-167T= (HFE)	ENSP00000315936.4:n.77-167T=
ENST00000353147.9:c.344T= (HFE)	ENSP00000312342.5:p.Val115=
ENST00000357618.9:c.884T= (HFE)	ENSP00000417404.1:p.Val295=
ENST00000397022.7:c.815T= (HFE)	ENSP00000380217.3:p.Val272=
ENST00000461397.5:c.842T= (HFE)	ENSP00000420802.1:p.Val281=
ENST00000470149.5:c.875T= (HFE)	ENSP00000419725.1:p.Val292=
ENST00000483782.1:n.1215T= (HFE)
ENST00000485729.1:c.5T= (HFE)	ENSP00000417534.1:p.Val2=
ENST00000486147.1:n.727T= (HFE)
ENST00000488199.5:c.578T= (HFE)	ENSP00000420559.1:p.Val193=
ENST00000629531.1:c.132+30821A= (H2BC3)	ENSP00000486472.1:n.132+30821A=
NM_000410.3:c.884T= , LRG_748t1:c.884T= (HFE)	NP_000401.1:p.Val295=
NM_001300749.1:c.884T= (HFE)	NP_001287678.1:p.Val295=
NM_139003.2:c.566T= (HFE)	NP_620572.1:p.Val189=
NM_139004.2:c.608T= (HFE)	NP_620573.1:p.Val203=
NM_139006.2:c.842T= (HFE)	NP_620575.1:p.Val281=
NM_139007.2:c.620T= (HFE)	NP_620576.1:p.Val207=
NM_139008.2:c.578T= (HFE)	NP_620577.1:p.Val193=
NM_139009.2:c.815T= (HFE)	NP_620578.1:p.Val272=
NM_139010.2:c.344T= (HFE)	NP_620579.1:p.Val115=
NM_139011.2:c.77-167T= (HFE)	NP_620580.1:n.77-167T=
XM_011514543.1:c.884T= (HFE)	XP_011512845.1:p.Val295=
XM_011514544.1:c.875T= (HFE)	XP_011512846.1:p.Val292=
XR_241893.2:n.1006T= (HFE)
XM_011514543.3:c.884T= (HFE)	XP_011512845.1:p.Val295=
XR_241893.4:n.978T= (HFE)
NM_001300749.2:c.884T= (HFE)	NP_001287678.1:p.Val295=
NM_139003.3:c.566T= (HFE)	NP_620572.1:p.Val189=
NM_139004.3:c.608T= (HFE)	NP_620573.1:p.Val203=
NM_139006.3:c.842T= (HFE)	NP_620575.1:p.Val281=
NM_139007.3:c.620T= (HFE)	NP_620576.1:p.Val207=
NM_139008.3:c.578T= (HFE)	NP_620577.1:p.Val193=
NM_139009.3:c.815T= (HFE)	NP_620578.1:p.Val272=
NM_139010.3:c.344T= (HFE)	NP_620579.1:p.Val115=
NM_139011.3:c.77-167T= (HFE)	NP_620580.1:n.77-167T=
NM_000410.4:c.884T= (HFE) MANE Select	NP_000401.1:p.Val295=
NM_001384164.1:c.884T= (HFE)	NP_001371093.1:p.Val295=