Canonical Allele Identifier: CA413604321

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.78033819C>A , CM000685.2:g.78033819C>A GRCh38
NC_000023.10:g.77289317C>A , CM000685.1:g.77289317C>A GRCh37
NC_000023.9:g.77175973C>A NCBI36
NG_013224.2:g.128123C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000343533.10:c.3539C>A (ATP7A) ENSP00000343026.6:p.Ser1180Ter
ENST00000682475.1:n.1926C>A (ATP7A)
ENST00000685033.1:c.773C>A (ATP7A) ENSP00000509269.1:p.Ser258Ter
ENST00000685264.1:c.3509C>A (ATP7A) ENSP00000510136.1:p.Ser1170Ter
ENST00000686033.1:c.3314C>A (ATP7A) ENSP00000510693.1:p.Ser1105Ter
ENST00000686133.1:c.3509C>A (ATP7A) ENSP00000509233.1:p.Ser1170Ter
ENST00000686255.1:n.2540C>A (ATP7A)
ENST00000686543.1:c.3275C>A (ATP7A) ENSP00000509477.1:p.Ser1092Ter
ENST00000687086.1:c.3509C>A (ATP7A) ENSP00000509566.1:p.Ser1170Ter
ENST00000689514.1:n.1551C>A (ATP7A)
ENST00000689767.1:c.3602C>A (ATP7A) ENSP00000509406.1:p.Ser1201Ter
ENST00000692908.1:c.3275C>A (ATP7A) ENSP00000508627.1:p.Ser1092Ter
ENST00000341514.11:c.3509C>A (ATP7A) MANE Select ENSP00000345728.6:p.Ser1170Ter
ENST00000644362.1:c.-19-76048C>A (PGK1) ENSP00000496140.1:n.-19-76048C>A
ENST00000645094.1:c.*3423C>A (ATP7A) ENSP00000493605.1:n.*3423C>A
ENST00000341514.10:c.3509C>A (ATP7A) ENSP00000345728.6:p.Ser1170Ter
ENST00000343533.9:c.3275C>A (ATP7A) ENSP00000343026.5:p.Ser1092Ter
ENST00000350425.5:c.*2682C>A (ATP7A) ENSP00000343678.5:n.*2682C>A
NM_000052.6:c.3509C>A (ATP7A) NP_000043.4:p.Ser1170Ter
NM_001282224.1:c.3275C>A (ATP7A) NP_001269153.1:p.Ser1092Ter
NR_104109.1:n.719C>A (ATP7A)
NM_000052.7:c.3509C>A (ATP7A) MANE Select NP_000043.4:p.Ser1170Ter
NR_104109.2:n.682C>A (ATP7A)
NM_001282224.2:c.3275C>A (ATP7A) NP_001269153.1:p.Ser1092Ter