Canonical Allele Identifier: CA2695235706

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.78013019dup , CM000685.2:g.78013019dup GRCh38
NC_000023.10:g.77268516dup , CM000685.1:g.77268516dup GRCh37
NC_000023.9:g.77155172dup NCBI36
NG_013224.2:g.107323dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000343533.10:c.2343dup (ATP7A) ENSP00000343026.6:p.Arg782GlufsTer11
ENST00000682475.1:n.823+1345dup (ATP7A)
ENST00000685264.1:c.2313dup (ATP7A) ENSP00000510136.1:p.Arg772GlufsTer11
ENST00000686033.1:c.2313dup (ATP7A) ENSP00000510693.1:p.Arg772GlufsTer11
ENST00000686133.1:c.2313dup (ATP7A) ENSP00000509233.1:p.Arg772GlufsTer11
ENST00000686255.1:n.1344dup (ATP7A)
ENST00000686480.1:c.2172+1345dup (ATP7A) ENSP00000508978.1:n.2172+1345dup
ENST00000686543.1:c.2172+1345dup (ATP7A) ENSP00000509477.1:n.2172+1345dup
ENST00000686688.1:c.2313dup (ATP7A) ENSP00000509416.1:p.Arg772GlufsTer11
ENST00000687086.1:c.2313dup (ATP7A) ENSP00000509566.1:p.Arg772GlufsTer11
ENST00000688746.1:n.3669dup (ATP7A)
ENST00000689514.1:n.355dup (ATP7A)
ENST00000689530.1:c.2313dup (ATP7A) ENSP00000509707.1:p.Arg772GlufsTer11
ENST00000689649.1:c.2313dup (ATP7A) ENSP00000509277.1:p.Arg772GlufsTer11
ENST00000689767.1:c.2406dup (ATP7A) ENSP00000509406.1:p.Arg803GlufsTer11
ENST00000689872.1:c.*262dup (ATP7A) ENSP00000509373.1:n.*262dup
ENST00000692908.1:c.2172+1345dup (ATP7A) ENSP00000508627.1:n.2172+1345dup
ENST00000693398.1:c.2313dup (ATP7A) ENSP00000510089.1:p.Arg772GlufsTer11
ENST00000341514.11:c.2313dup (ATP7A) MANE Select ENSP00000345728.6:p.Arg772GlufsTer11
ENST00000644362.1:c.-19-96848dup (PGK1) ENSP00000496140.1:n.-19-96848dup
ENST00000645094.1:c.*2227dup (ATP7A) ENSP00000493605.1:n.*2227dup
ENST00000341514.10:c.2313dup (ATP7A) ENSP00000345728.6:p.Arg772GlufsTer11
ENST00000343533.9:c.2172+1345dup (ATP7A) ENSP00000343026.5:n.2172+1345dup
ENST00000350425.5:c.*1486dup (ATP7A) ENSP00000343678.5:n.*1486dup
NM_000052.6:c.2313dup (ATP7A) NP_000043.4:p.Arg772GlufsTer11
NM_001282224.1:c.2172+1345dup (ATP7A) NP_001269153.1:n.2172+1345dup
NR_104109.1:n.322-18381dup (ATP7A)
NM_000052.7:c.2313dup (ATP7A) MANE Select NP_000043.4:p.Arg772GlufsTer11
NR_104109.2:n.285-18381dup (ATP7A)
NM_001282224.2:c.2172+1345dup (ATP7A) NP_001269153.1:n.2172+1345dup