Canonical Allele Identifier: CA363207669

Gene: HFE H2BC4 H2BC3

Linked Data

• MyVariant Identifiers: chr6:g.26092951T>A (hg19) ; chr6:g.26092723T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.26092723T>A , CM000668.2:g.26092723T>A	GRCh38
NC_000006.11:g.26092951T>A , CM000668.1:g.26092951T>A	GRCh37
NC_000006.10:g.26200930T>A	NCBI36
NG_008720.2:g.10443T>A , LRG_748:g.10443T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000485729.2:c.655T>A (HFE)	ENSP00000417534.2:p.Ser219Thr
ENST00000707188.1:c.391-1689A>T (H2BC4)	ENSP00000516775.1:n.391-1689A>T
ENST00000357618.10:c.655T>A (HFE) MANE Select	ENSP00000417404.1:p.Ser219Thr
ENST00000309234.10:c.655T>A (HFE)	ENSP00000311698.6:p.Ser219Thr
ENST00000317896.11:c.379T>A (HFE)	ENSP00000313776.7:p.Ser127Thr
ENST00000336625.12:c.341-4T>A (HFE)	ENSP00000337819.8:n.341-4T>A
ENST00000349999.8:c.391T>A (HFE)	ENSP00000259699.6:p.Ser131Thr
ENST00000352392.8:c.77-396T>A (HFE)	ENSP00000315936.4:n.77-396T>A
ENST00000353147.9:c.115T>A (HFE)	ENSP00000312342.5:p.Ser39Thr
ENST00000357618.9:c.655T>A (HFE)	ENSP00000417404.1:p.Ser219Thr
ENST00000397022.7:c.586T>A (HFE)	ENSP00000380217.3:p.Ser196Thr
ENST00000461397.5:c.617-4T>A (HFE)	ENSP00000420802.1:n.617-4T>A
ENST00000470149.5:c.650-4T>A (HFE)	ENSP00000419725.1:n.650-4T>A
ENST00000483782.1:n.986T>A (HFE)
ENST00000486147.1:n.498T>A (HFE)
ENST00000488199.5:c.353-4T>A (HFE)	ENSP00000420559.1:n.353-4T>A
ENST00000629531.1:c.132+31050A>T (H2BC3)	ENSP00000486472.1:n.132+31050A>T
NM_000410.3:c.655T>A , LRG_748t1:c.655T>A (HFE)	NP_000401.1:p.Ser219Thr
NM_001300749.1:c.655T>A (HFE)	NP_001287678.1:p.Ser219Thr
NM_139003.2:c.341-4T>A (HFE)	NP_620572.1:n.341-4T>A
NM_139004.2:c.379T>A (HFE)	NP_620573.1:p.Ser127Thr
NM_139006.2:c.617-4T>A (HFE)	NP_620575.1:n.617-4T>A
NM_139007.2:c.391T>A (HFE)	NP_620576.1:p.Ser131Thr
NM_139008.2:c.353-4T>A (HFE)	NP_620577.1:n.353-4T>A
NM_139009.2:c.586T>A (HFE)	NP_620578.1:p.Ser196Thr
NM_139010.2:c.115T>A (HFE)	NP_620579.1:p.Ser39Thr
NM_139011.2:c.77-396T>A (HFE)	NP_620580.1:n.77-396T>A
XM_011514543.1:c.655T>A (HFE)	XP_011512845.1:p.Ser219Thr
XM_011514544.1:c.650-4T>A (HFE)	XP_011512846.1:n.650-4T>A
XR_241893.2:n.777T>A (HFE)
XM_011514543.3:c.655T>A (HFE)	XP_011512845.1:p.Ser219Thr
XR_241893.4:n.749T>A (HFE)
NM_001300749.2:c.655T>A (HFE)	NP_001287678.1:p.Ser219Thr
NM_139003.3:c.341-4T>A (HFE)	NP_620572.1:n.341-4T>A
NM_139004.3:c.379T>A (HFE)	NP_620573.1:p.Ser127Thr
NM_139006.3:c.617-4T>A (HFE)	NP_620575.1:n.617-4T>A
NM_139007.3:c.391T>A (HFE)	NP_620576.1:p.Ser131Thr
NM_139008.3:c.353-4T>A (HFE)	NP_620577.1:n.353-4T>A
NM_139009.3:c.586T>A (HFE)	NP_620578.1:p.Ser196Thr
NM_139010.3:c.115T>A (HFE)	NP_620579.1:p.Ser39Thr
NM_139011.3:c.77-396T>A (HFE)	NP_620580.1:n.77-396T>A
NM_000410.4:c.655T>A (HFE) MANE Select	NP_000401.1:p.Ser219Thr
NM_001384164.1:c.655T>A (HFE)	NP_001371093.1:p.Ser219Thr