Canonical Allele Identifier: CA363208680

Gene: HFE H2BC4 H2BC3

Linked Data

• gnomAD v4: 6-26092930-G-T
• MyVariant Identifiers: chr6:g.26093158G>T (hg19) ; chr6:g.26092930G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.26092930G>T , CM000668.2:g.26092930G>T	GRCh38
NC_000006.11:g.26093158G>T , CM000668.1:g.26093158G>T	GRCh37
NC_000006.10:g.26201137G>T	NCBI36
NG_008720.2:g.10650G>T , LRG_748:g.10650G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000485729.2:c.862G>T (HFE)	ENSP00000417534.2:p.Gly288Cys
ENST00000707188.1:c.391-1896C>A (H2BC4)	ENSP00000516775.1:n.391-1896C>A
ENST00000357618.10:c.862G>T (HFE) MANE Select	ENSP00000417404.1:p.Gly288Cys
ENST00000309234.10:c.862G>T (HFE)	ENSP00000311698.6:p.Gly288Cys
ENST00000317896.11:c.586G>T (HFE)	ENSP00000313776.7:p.Gly196Cys
ENST00000336625.12:c.544G>T (HFE)	ENSP00000337819.8:p.Gly182Cys
ENST00000349999.8:c.598G>T (HFE)	ENSP00000259699.6:p.Gly200Cys
ENST00000352392.8:c.77-189G>T (HFE)	ENSP00000315936.4:n.77-189G>T
ENST00000353147.9:c.322G>T (HFE)	ENSP00000312342.5:p.Gly108Cys
ENST00000357618.9:c.862G>T (HFE)	ENSP00000417404.1:p.Gly288Cys
ENST00000397022.7:c.793G>T (HFE)	ENSP00000380217.3:p.Gly265Cys
ENST00000461397.5:c.820G>T (HFE)	ENSP00000420802.1:p.Gly274Cys
ENST00000470149.5:c.853G>T (HFE)	ENSP00000419725.1:p.Gly285Cys
ENST00000483782.1:n.1193G>T (HFE)
ENST00000486147.1:n.705G>T (HFE)
ENST00000488199.5:c.556G>T (HFE)	ENSP00000420559.1:p.Gly186Cys
ENST00000629531.1:c.132+30843C>A (H2BC3)	ENSP00000486472.1:n.132+30843C>A
NM_000410.3:c.862G>T , LRG_748t1:c.862G>T (HFE)	NP_000401.1:p.Gly288Cys
NM_001300749.1:c.862G>T (HFE)	NP_001287678.1:p.Gly288Cys
NM_139003.2:c.544G>T (HFE)	NP_620572.1:p.Gly182Cys
NM_139004.2:c.586G>T (HFE)	NP_620573.1:p.Gly196Cys
NM_139006.2:c.820G>T (HFE)	NP_620575.1:p.Gly274Cys
NM_139007.2:c.598G>T (HFE)	NP_620576.1:p.Gly200Cys
NM_139008.2:c.556G>T (HFE)	NP_620577.1:p.Gly186Cys
NM_139009.2:c.793G>T (HFE)	NP_620578.1:p.Gly265Cys
NM_139010.2:c.322G>T (HFE)	NP_620579.1:p.Gly108Cys
NM_139011.2:c.77-189G>T (HFE)	NP_620580.1:n.77-189G>T
XM_011514543.1:c.862G>T (HFE)	XP_011512845.1:p.Gly288Cys
XM_011514544.1:c.853G>T (HFE)	XP_011512846.1:p.Gly285Cys
XR_241893.2:n.984G>T (HFE)
XM_011514543.3:c.862G>T (HFE)	XP_011512845.1:p.Gly288Cys
XR_241893.4:n.956G>T (HFE)
NM_001300749.2:c.862G>T (HFE)	NP_001287678.1:p.Gly288Cys
NM_139003.3:c.544G>T (HFE)	NP_620572.1:p.Gly182Cys
NM_139004.3:c.586G>T (HFE)	NP_620573.1:p.Gly196Cys
NM_139006.3:c.820G>T (HFE)	NP_620575.1:p.Gly274Cys
NM_139007.3:c.598G>T (HFE)	NP_620576.1:p.Gly200Cys
NM_139008.3:c.556G>T (HFE)	NP_620577.1:p.Gly186Cys
NM_139009.3:c.793G>T (HFE)	NP_620578.1:p.Gly265Cys
NM_139010.3:c.322G>T (HFE)	NP_620579.1:p.Gly108Cys
NM_139011.3:c.77-189G>T (HFE)	NP_620580.1:n.77-189G>T
NM_000410.4:c.862G>T (HFE) MANE Select	NP_000401.1:p.Gly288Cys
NM_001384164.1:c.862G>T (HFE)	NP_001371093.1:p.Gly288Cys