Canonical Allele Identifier: CA413603864

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.78033617G>A , CM000685.2:g.78033617G>A GRCh38
NC_000023.10:g.77289115G>A , CM000685.1:g.77289115G>A GRCh37
NC_000023.9:g.77175771G>A NCBI36
NG_013224.2:g.127921G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000343533.10:c.3337G>A (ATP7A) ENSP00000343026.6:p.Glu1113Lys
ENST00000682475.1:n.1724G>A (ATP7A)
ENST00000685033.1:c.571G>A (ATP7A) ENSP00000509269.1:p.Glu191Lys
ENST00000685264.1:c.3307G>A (ATP7A) ENSP00000510136.1:p.Glu1103Lys
ENST00000686033.1:c.3112G>A (ATP7A) ENSP00000510693.1:p.Glu1038Lys
ENST00000686133.1:c.3307G>A (ATP7A) ENSP00000509233.1:p.Glu1103Lys
ENST00000686255.1:n.2338G>A (ATP7A)
ENST00000686543.1:c.3073G>A (ATP7A) ENSP00000509477.1:p.Glu1025Lys
ENST00000687086.1:c.3307G>A (ATP7A) ENSP00000509566.1:p.Glu1103Lys
ENST00000689514.1:n.1349G>A (ATP7A)
ENST00000689767.1:c.3400G>A (ATP7A) ENSP00000509406.1:p.Glu1134Lys
ENST00000692908.1:c.3073G>A (ATP7A) ENSP00000508627.1:p.Glu1025Lys
ENST00000341514.11:c.3307G>A (ATP7A) MANE Select ENSP00000345728.6:p.Glu1103Lys
ENST00000644362.1:c.-19-76250G>A (PGK1) ENSP00000496140.1:n.-19-76250G>A
ENST00000645094.1:c.*3221G>A (ATP7A) ENSP00000493605.1:n.*3221G>A
ENST00000341514.10:c.3307G>A (ATP7A) ENSP00000345728.6:p.Glu1103Lys
ENST00000343533.9:c.3073G>A (ATP7A) ENSP00000343026.5:p.Glu1025Lys
ENST00000350425.5:c.*2480G>A (ATP7A) ENSP00000343678.5:n.*2480G>A
NM_000052.6:c.3307G>A (ATP7A) NP_000043.4:p.Glu1103Lys
NM_001282224.1:c.3073G>A (ATP7A) NP_001269153.1:p.Glu1025Lys
NR_104109.1:n.517G>A (ATP7A)
NM_000052.7:c.3307G>A (ATP7A) MANE Select NP_000043.4:p.Glu1103Lys
NR_104109.2:n.480G>A (ATP7A)
NM_001282224.2:c.3073G>A (ATP7A) NP_001269153.1:p.Glu1025Lys