Canonical Allele Identifier: CA413603870

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.78033619A>C , CM000685.2:g.78033619A>C GRCh38
NC_000023.10:g.77289117A>C , CM000685.1:g.77289117A>C GRCh37
NC_000023.9:g.77175773A>C NCBI36
NG_013224.2:g.127923A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000343533.10:c.3339A>C (ATP7A) ENSP00000343026.6:p.Glu1113Asp
ENST00000682475.1:n.1726A>C (ATP7A)
ENST00000685033.1:c.573A>C (ATP7A) ENSP00000509269.1:p.Glu191Asp
ENST00000685264.1:c.3309A>C (ATP7A) ENSP00000510136.1:p.Glu1103Asp
ENST00000686033.1:c.3114A>C (ATP7A) ENSP00000510693.1:p.Glu1038Asp
ENST00000686133.1:c.3309A>C (ATP7A) ENSP00000509233.1:p.Glu1103Asp
ENST00000686255.1:n.2340A>C (ATP7A)
ENST00000686543.1:c.3075A>C (ATP7A) ENSP00000509477.1:p.Glu1025Asp
ENST00000687086.1:c.3309A>C (ATP7A) ENSP00000509566.1:p.Glu1103Asp
ENST00000689514.1:n.1351A>C (ATP7A)
ENST00000689767.1:c.3402A>C (ATP7A) ENSP00000509406.1:p.Glu1134Asp
ENST00000692908.1:c.3075A>C (ATP7A) ENSP00000508627.1:p.Glu1025Asp
ENST00000341514.11:c.3309A>C (ATP7A) MANE Select ENSP00000345728.6:p.Glu1103Asp
ENST00000644362.1:c.-19-76248A>C (PGK1) ENSP00000496140.1:n.-19-76248A>C
ENST00000645094.1:c.*3223A>C (ATP7A) ENSP00000493605.1:n.*3223A>C
ENST00000341514.10:c.3309A>C (ATP7A) ENSP00000345728.6:p.Glu1103Asp
ENST00000343533.9:c.3075A>C (ATP7A) ENSP00000343026.5:p.Glu1025Asp
ENST00000350425.5:c.*2482A>C (ATP7A) ENSP00000343678.5:n.*2482A>C
NM_000052.6:c.3309A>C (ATP7A) NP_000043.4:p.Glu1103Asp
NM_001282224.1:c.3075A>C (ATP7A) NP_001269153.1:p.Glu1025Asp
NR_104109.1:n.519A>C (ATP7A)
NM_000052.7:c.3309A>C (ATP7A) MANE Select NP_000043.4:p.Glu1103Asp
NR_104109.2:n.482A>C (ATP7A)
NM_001282224.2:c.3075A>C (ATP7A) NP_001269153.1:p.Glu1025Asp