Canonical Allele Identifier: CA413604115

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.78033727C>A , CM000685.2:g.78033727C>A GRCh38
NC_000023.10:g.77289225C>A , CM000685.1:g.77289225C>A GRCh37
NC_000023.9:g.77175881C>A NCBI36
NG_013224.2:g.128031C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000343533.10:c.3447C>A (ATP7A) ENSP00000343026.6:p.Asp1149Glu
ENST00000682475.1:n.1834C>A (ATP7A)
ENST00000685033.1:c.681C>A (ATP7A) ENSP00000509269.1:p.Asp227Glu
ENST00000685264.1:c.3417C>A (ATP7A) ENSP00000510136.1:p.Asp1139Glu
ENST00000686033.1:c.3222C>A (ATP7A) ENSP00000510693.1:p.Asp1074Glu
ENST00000686133.1:c.3417C>A (ATP7A) ENSP00000509233.1:p.Asp1139Glu
ENST00000686255.1:n.2448C>A (ATP7A)
ENST00000686543.1:c.3183C>A (ATP7A) ENSP00000509477.1:p.Asp1061Glu
ENST00000687086.1:c.3417C>A (ATP7A) ENSP00000509566.1:p.Asp1139Glu
ENST00000689514.1:n.1459C>A (ATP7A)
ENST00000689767.1:c.3510C>A (ATP7A) ENSP00000509406.1:p.Asp1170Glu
ENST00000692908.1:c.3183C>A (ATP7A) ENSP00000508627.1:p.Asp1061Glu
ENST00000341514.11:c.3417C>A (ATP7A) MANE Select ENSP00000345728.6:p.Asp1139Glu
ENST00000644362.1:c.-19-76140C>A (PGK1) ENSP00000496140.1:n.-19-76140C>A
ENST00000645094.1:c.*3331C>A (ATP7A) ENSP00000493605.1:n.*3331C>A
ENST00000341514.10:c.3417C>A (ATP7A) ENSP00000345728.6:p.Asp1139Glu
ENST00000343533.9:c.3183C>A (ATP7A) ENSP00000343026.5:p.Asp1061Glu
ENST00000350425.5:c.*2590C>A (ATP7A) ENSP00000343678.5:n.*2590C>A
NM_000052.6:c.3417C>A (ATP7A) NP_000043.4:p.Asp1139Glu
NM_001282224.1:c.3183C>A (ATP7A) NP_001269153.1:p.Asp1061Glu
NR_104109.1:n.627C>A (ATP7A)
NM_000052.7:c.3417C>A (ATP7A) MANE Select NP_000043.4:p.Asp1139Glu
NR_104109.2:n.590C>A (ATP7A)
NM_001282224.2:c.3183C>A (ATP7A) NP_001269153.1:p.Asp1061Glu