Canonical Allele Identifier: CA1616887492

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.26087426G= , CM000668.2:g.26087426G= GRCh38
NC_000006.11:g.26087654G= , CM000668.1:g.26087654G= GRCh37
NC_000006.10:g.26195633G= NCBI36
NG_008720.2:g.5146G= , LRG_748:g.5146G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000707188.1:c.1439C= (H2BC4) ENSP00000516775.1:n.1439C=
ENST00000317896.11:c.-15G= (HFE) ENSP00000313776.7:n.-15G=
ENST00000336625.12:c.-15G= (HFE) ENSP00000337819.8:n.-15G=
ENST00000349999.8:c.-15G= (HFE) ENSP00000259699.6:n.-15G=
ENST00000352392.8:c.-15G= (HFE) ENSP00000315936.4:n.-15G=
ENST00000353147.9:c.-15G= (HFE) ENSP00000312342.5:n.-15G=
ENST00000357618.9:c.-15G= (HFE) ENSP00000417404.1:n.-15G=
ENST00000397022.7:c.-15G= (HFE) ENSP00000380217.3:n.-15G=
ENST00000461397.5:c.-15G= (HFE) ENSP00000420802.1:n.-15G=
ENST00000470149.5:c.-15G= (HFE) ENSP00000419725.1:n.-15G=
ENST00000483782.1:n.108G= (HFE)
ENST00000486147.1:n.29G= (HFE)
ENST00000488199.5:c.-15G= (HFE) ENSP00000420559.1:n.-15G=
ENST00000629531.1:c.132+36347C= (H2BC3) ENSP00000486472.1:n.132+36347C=
NM_000410.3:c.-15G= , LRG_748t1:c.-15G= (HFE) NP_000401.1:n.-15G=
NM_001300749.1:c.-15G= (HFE) NP_001287678.1:n.-15G=
NM_139003.2:c.-15G= (HFE) NP_620572.1:n.-15G=
NM_139004.2:c.-15G= (HFE) NP_620573.1:n.-15G=
NM_139006.2:c.-15G= (HFE) NP_620575.1:n.-15G=
NM_139007.2:c.-15G= (HFE) NP_620576.1:n.-15G=
NM_139008.2:c.-15G= (HFE) NP_620577.1:n.-15G=
NM_139009.2:c.-15G= (HFE) NP_620578.1:n.-15G=
NM_139010.2:c.-15G= (HFE) NP_620579.1:n.-15G=
NM_139011.2:c.-15G= (HFE) NP_620580.1:n.-15G=
XM_011514543.1:c.-15G= (HFE) XP_011512845.1:n.-15G=
XM_011514544.1:c.-15G= (HFE) XP_011512846.1:n.-15G=
XR_241893.2:n.108G= (HFE)
NR_144383.1:n.1049C= (HFE-AS1)
XM_011514543.3:c.-15G= (HFE) XP_011512845.1:n.-15G=
XR_241893.4:n.80G= (HFE)