Canonical Allele Identifier: CA2580074259

Gene: HFE H2BC4 H2BC3

Linked Data

• ClinVar Variation Id: 2445854
• ClinVar RCV Id: RCV003155773

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.26091046_26091047delinsTC , CM000668.2:g.26091046_26091047delinsTC	GRCh38
NC_000006.11:g.26091274_26091275delinsTC , CM000668.1:g.26091274_26091275delinsTC	GRCh37
NC_000006.10:g.26199253_26199254delinsTC	NCBI36
NG_008720.2:g.8766_8767delinsTC , LRG_748:g.8766_8767delinsTC

Transcript Alleles

HGVS	Amino-acid change
ENST00000485729.2:c.282_283delinsTC (HFE)	ENSP00000417534.2:p.Trp94_Asp95delinsCysH...
ENST00000707188.1:c.391-13_391-12delinsGA (H2BC4)	ENSP00000516775.1:n.391-13_391-12delinsGA...
ENST00000357618.10:c.282_283delinsTC (HFE) MANE Select	ENSP00000417404.1:p.Trp94_Asp95delinsCysH...
ENST00000309234.10:c.282_283delinsTC (HFE)	ENSP00000311698.6:p.Trp94_Asp95delinsCysH...
ENST00000317896.11:c.282_283delinsTC (HFE)	ENSP00000313776.7:p.Trp94_Asp95delinsCysH...
ENST00000336625.12:c.282_283delinsTC (HFE)	ENSP00000337819.8:p.Trp94_Asp95delinsCysH...
ENST00000349999.8:c.77-268_77-267delinsTC (HFE)	ENSP00000259699.6:n.77-268_77-267delinsTC...
ENST00000352392.8:c.77-2073_77-2072delinsTC (HFE)	ENSP00000315936.4:n.77-2073_77-2072delins...
ENST00000353147.9:c.77-1639_77-1638delinsTC (HFE)	ENSP00000312342.5:n.77-1639_77-1638delins...
ENST00000357618.9:c.282_283delinsTC (HFE)	ENSP00000417404.1:p.Trp94_Asp95delinsCysH...
ENST00000397022.7:c.213_214delinsTC (HFE)	ENSP00000380217.3:p.Trp71_Asp72delinsCysH...
ENST00000461397.5:c.282_283delinsTC (HFE)	ENSP00000420802.1:p.Trp94_Asp95delinsCysH...
ENST00000470149.5:c.282_283delinsTC (HFE)	ENSP00000419725.1:p.Trp94_Asp95delinsCysH...
ENST00000483782.1:n.404_405delinsTC (HFE)
ENST00000486147.1:n.325_326delinsTC (HFE)
ENST00000488199.5:c.77-268_77-267delinsTC (HFE)	ENSP00000420559.1:n.77-268_77-267delinsTC...
ENST00000629531.1:c.132+32726_132+32727delinsGA (H2BC3)	ENSP00000486472.1:n.132+32726_132+32727de...
NM_000410.3:c.282_283delinsTC , LRG_748t1:c.282_283delinsTC (HFE)	NP_000401.1:p.Trp94_Asp95delinsCysHis
NM_001300749.1:c.282_283delinsTC (HFE)	NP_001287678.1:p.Trp94_Asp95delinsCysHis
NM_139003.2:c.282_283delinsTC (HFE)	NP_620572.1:p.Trp94_Asp95delinsCysHis
NM_139004.2:c.282_283delinsTC (HFE)	NP_620573.1:p.Trp94_Asp95delinsCysHis
NM_139006.2:c.282_283delinsTC (HFE)	NP_620575.1:p.Trp94_Asp95delinsCysHis
NM_139007.2:c.77-268_77-267delinsTC (HFE)	NP_620576.1:n.77-268_77-267delinsTC
NM_139008.2:c.77-268_77-267delinsTC (HFE)	NP_620577.1:n.77-268_77-267delinsTC
NM_139009.2:c.213_214delinsTC (HFE)	NP_620578.1:p.Trp71_Asp72delinsCysHis
NM_139010.2:c.77-1639_77-1638delinsTC (HFE)	NP_620579.1:n.77-1639_77-1638delinsTC
NM_139011.2:c.77-2073_77-2072delinsTC (HFE)	NP_620580.1:n.77-2073_77-2072delinsTC
XM_011514543.1:c.282_283delinsTC (HFE)	XP_011512845.1:p.Trp94_Asp95delinsCysHis
XM_011514544.1:c.282_283delinsTC (HFE)	XP_011512846.1:p.Trp94_Asp95delinsCysHis
XR_241893.2:n.404_405delinsTC (HFE)
XM_011514543.3:c.282_283delinsTC (HFE)	XP_011512845.1:p.Trp94_Asp95delinsCysHis
XR_241893.4:n.376_377delinsTC (HFE)
NM_001300749.2:c.282_283delinsTC (HFE)	NP_001287678.1:p.Trp94_Asp95delinsCysHis
NM_139003.3:c.282_283delinsTC (HFE)	NP_620572.1:p.Trp94_Asp95delinsCysHis
NM_139004.3:c.282_283delinsTC (HFE)	NP_620573.1:p.Trp94_Asp95delinsCysHis
NM_139006.3:c.282_283delinsTC (HFE)	NP_620575.1:p.Trp94_Asp95delinsCysHis
NM_139007.3:c.77-268_77-267delinsTC (HFE)	NP_620576.1:n.77-268_77-267delinsTC
NM_139008.3:c.77-268_77-267delinsTC (HFE)	NP_620577.1:n.77-268_77-267delinsTC
NM_139009.3:c.213_214delinsTC (HFE)	NP_620578.1:p.Trp71_Asp72delinsCysHis
NM_139010.3:c.77-1639_77-1638delinsTC (HFE)	NP_620579.1:n.77-1639_77-1638delinsTC
NM_139011.3:c.77-2073_77-2072delinsTC (HFE)	NP_620580.1:n.77-2073_77-2072delinsTC
NM_000410.4:c.282_283delinsTC (HFE) MANE Select	NP_000401.1:p.Trp94_Asp95delinsCysHis
NM_001384164.1:c.282_283delinsTC (HFE)	NP_001371093.1:p.Trp94_Asp95delinsCysHis