Canonical Allele Identifier: CA1616889916

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.26092827_26092828delinsTA , CM000668.2:g.26092827_26092828delinsTA GRCh38
NC_000006.11:g.26093055_26093056delinsTA , CM000668.1:g.26093055_26093056delinsTA GRCh37
NC_000006.10:g.26201034_26201035delinsTA NCBI36
NG_008720.2:g.10547_10548delinsTA , LRG_748:g.10547_10548delinsTA

Transcript Alleles

HGVS Amino-acid change
ENST00000485729.2:c.759_760delinsTA (HFE) ENSP00000417534.2:p.Pro253=
ENST00000707188.1:c.391-1794_391-1793delinsTA (H2BC4) ENSP00000516775.1:n.391-1794_391-1793deli...
ENST00000357618.10:c.759_760delinsTA (HFE) MANE Select ENSP00000417404.1:p.Pro253=
ENST00000309234.10:c.759_760delinsTA (HFE) ENSP00000311698.6:p.Pro253=
ENST00000317896.11:c.483_484delinsTA (HFE) ENSP00000313776.7:p.Pro161=
ENST00000336625.12:c.441_442delinsTA (HFE) ENSP00000337819.8:p.Pro147=
ENST00000349999.8:c.495_496delinsTA (HFE) ENSP00000259699.6:p.Pro165=
ENST00000352392.8:c.77-292_77-291delinsTA (HFE) ENSP00000315936.4:n.77-292_77-291delinsTA...
ENST00000353147.9:c.219_220delinsTA (HFE) ENSP00000312342.5:p.Pro73=
ENST00000357618.9:c.759_760delinsTA (HFE) ENSP00000417404.1:p.Pro253=
ENST00000397022.7:c.690_691delinsTA (HFE) ENSP00000380217.3:p.Pro230=
ENST00000461397.5:c.717_718delinsTA (HFE) ENSP00000420802.1:p.Pro239=
ENST00000470149.5:c.750_751delinsTA (HFE) ENSP00000419725.1:p.Pro250=
ENST00000483782.1:n.1090_1091delinsTA (HFE)
ENST00000486147.1:n.602_603delinsTA (HFE)
ENST00000488199.5:c.453_454delinsTA (HFE) ENSP00000420559.1:p.Pro151=
ENST00000629531.1:c.132+30945_132+30946delinsTA (H2BC3) ENSP00000486472.1:n.132+30945_132+30946de...
NM_000410.3:c.759_760delinsTA , LRG_748t1:c.759_760delinsTA (HFE) NP_000401.1:p.Pro253=
NM_001300749.1:c.759_760delinsTA (HFE) NP_001287678.1:p.Pro253=
NM_139003.2:c.441_442delinsTA (HFE) NP_620572.1:p.Pro147=
NM_139004.2:c.483_484delinsTA (HFE) NP_620573.1:p.Pro161=
NM_139006.2:c.717_718delinsTA (HFE) NP_620575.1:p.Pro239=
NM_139007.2:c.495_496delinsTA (HFE) NP_620576.1:p.Pro165=
NM_139008.2:c.453_454delinsTA (HFE) NP_620577.1:p.Pro151=
NM_139009.2:c.690_691delinsTA (HFE) NP_620578.1:p.Pro230=
NM_139010.2:c.219_220delinsTA (HFE) NP_620579.1:p.Pro73=
NM_139011.2:c.77-292_77-291delinsTA (HFE) NP_620580.1:n.77-292_77-291delinsTA
XM_011514543.1:c.759_760delinsTA (HFE) XP_011512845.1:p.Pro253=
XM_011514544.1:c.750_751delinsTA (HFE) XP_011512846.1:p.Pro250=
XR_241893.2:n.881_882delinsTA (HFE)
XM_011514543.3:c.759_760delinsTA (HFE) XP_011512845.1:p.Pro253=
XR_241893.4:n.853_854delinsTA (HFE)
NM_001300749.2:c.759_760delinsTA (HFE) NP_001287678.1:p.Pro253=
NM_139003.3:c.441_442delinsTA (HFE) NP_620572.1:p.Pro147=
NM_139004.3:c.483_484delinsTA (HFE) NP_620573.1:p.Pro161=
NM_139006.3:c.717_718delinsTA (HFE) NP_620575.1:p.Pro239=
NM_139007.3:c.495_496delinsTA (HFE) NP_620576.1:p.Pro165=
NM_139008.3:c.453_454delinsTA (HFE) NP_620577.1:p.Pro151=
NM_139009.3:c.690_691delinsTA (HFE) NP_620578.1:p.Pro230=
NM_139010.3:c.219_220delinsTA (HFE) NP_620579.1:p.Pro73=
NM_139011.3:c.77-292_77-291delinsTA (HFE) NP_620580.1:n.77-292_77-291delinsTA
NM_000410.4:c.759_760delinsTA (HFE) MANE Select NP_000401.1:p.Pro253=
NM_001384164.1:c.759_760delinsTA (HFE) NP_001371093.1:p.Pro253=