Canonical Allele Identifier: CA2677605485

Linked Data

gnomAD v4: 6-26093037-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.26093037C>T , CM000668.2:g.26093037C>T GRCh38
NC_000006.11:g.26093265C>T , CM000668.1:g.26093265C>T GRCh37
NC_000006.10:g.26201244C>T NCBI36
NG_008720.2:g.10757C>T , LRG_748:g.10757C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000485729.2:c.892+77C>T (HFE) ENSP00000417534.2:n.892+77C>T
ENST00000707188.1:c.391-2003G>A (H2BC4) ENSP00000516775.1:n.391-2003G>A
ENST00000357618.10:c.892+77C>T (HFE) MANE Select ENSP00000417404.1:n.892+77C>T
ENST00000309234.10:c.892+77C>T (HFE) ENSP00000311698.6:n.892+77C>T
ENST00000317896.11:c.616+77C>T (HFE) ENSP00000313776.7:n.616+77C>T
ENST00000336625.12:c.574+77C>T (HFE) ENSP00000337819.8:n.574+77C>T
ENST00000349999.8:c.628+77C>T (HFE) ENSP00000259699.6:n.628+77C>T
ENST00000352392.8:c.77-82C>T (HFE) ENSP00000315936.4:n.77-82C>T
ENST00000353147.9:c.352+77C>T (HFE) ENSP00000312342.5:n.352+77C>T
ENST00000357618.9:c.892+77C>T (HFE) ENSP00000417404.1:n.892+77C>T
ENST00000397022.7:c.823+77C>T (HFE) ENSP00000380217.3:n.823+77C>T
ENST00000461397.5:c.850+77C>T (HFE) ENSP00000420802.1:n.850+77C>T
ENST00000470149.5:c.883+77C>T (HFE) ENSP00000419725.1:n.883+77C>T
ENST00000485729.1:c.13+77C>T (HFE) ENSP00000417534.1:n.13+77C>T
ENST00000486147.1:n.801+11C>T (HFE)
ENST00000488199.5:c.586+77C>T (HFE) ENSP00000420559.1:n.586+77C>T
ENST00000629531.1:c.132+30736G>A (H2BC3) ENSP00000486472.1:n.132+30736G>A
NM_000410.3:c.892+77C>T , LRG_748t1:c.892+77C>T (HFE) NP_000401.1:n.892+77C>T
NM_001300749.1:c.892+77C>T (HFE) NP_001287678.1:n.892+77C>T
NM_139003.2:c.574+77C>T (HFE) NP_620572.1:n.574+77C>T
NM_139004.2:c.616+77C>T (HFE) NP_620573.1:n.616+77C>T
NM_139006.2:c.850+77C>T (HFE) NP_620575.1:n.850+77C>T
NM_139007.2:c.628+77C>T (HFE) NP_620576.1:n.628+77C>T
NM_139008.2:c.586+77C>T (HFE) NP_620577.1:n.586+77C>T
NM_139009.2:c.823+77C>T (HFE) NP_620578.1:n.823+77C>T
NM_139010.2:c.352+77C>T (HFE) NP_620579.1:n.352+77C>T
NM_139011.2:c.77-82C>T (HFE) NP_620580.1:n.77-82C>T
XM_011514543.1:c.892+77C>T (HFE) XP_011512845.1:n.892+77C>T
XM_011514544.1:c.883+77C>T (HFE) XP_011512846.1:n.883+77C>T
XR_241893.2:n.1080+11C>T (HFE)
XM_011514543.3:c.892+77C>T (HFE) XP_011512845.1:n.892+77C>T
XR_241893.4:n.1052+11C>T (HFE)
NM_001300749.2:c.892+77C>T (HFE) NP_001287678.1:n.892+77C>T
NM_139003.3:c.574+77C>T (HFE) NP_620572.1:n.574+77C>T
NM_139004.3:c.616+77C>T (HFE) NP_620573.1:n.616+77C>T
NM_139006.3:c.850+77C>T (HFE) NP_620575.1:n.850+77C>T
NM_139007.3:c.628+77C>T (HFE) NP_620576.1:n.628+77C>T
NM_139008.3:c.586+77C>T (HFE) NP_620577.1:n.586+77C>T
NM_139009.3:c.823+77C>T (HFE) NP_620578.1:n.823+77C>T
NM_139010.3:c.352+77C>T (HFE) NP_620579.1:n.352+77C>T
NM_139011.3:c.77-82C>T (HFE) NP_620580.1:n.77-82C>T
NM_000410.4:c.892+77C>T (HFE) MANE Select NP_000401.1:n.892+77C>T
NM_001384164.1:c.892+77C>T (HFE) NP_001371093.1:n.892+77C>T