Canonical Allele Identifier: CA2821937215

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.78011014A>G , CM000685.2:g.78011014A>G GRCh38
NC_000023.10:g.77266511A>G , CM000685.1:g.77266511A>G GRCh37
NC_000023.9:g.77153167A>G NCBI36
NG_013224.2:g.105318A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000343533.10:c.1900-162A>G (ATP7A) ENSP00000343026.6:n.1900-162A>G
ENST00000682475.1:n.163A>G (ATP7A)
ENST00000685264.1:c.1870-162A>G (ATP7A) ENSP00000510136.1:n.1870-162A>G
ENST00000686033.1:c.1870-162A>G (ATP7A) ENSP00000510693.1:n.1870-162A>G
ENST00000686133.1:c.1870-162A>G (ATP7A) ENSP00000509233.1:n.1870-162A>G
ENST00000686255.1:n.543A>G (ATP7A)
ENST00000686480.1:c.1870-162A>G (ATP7A) ENSP00000508978.1:n.1870-162A>G
ENST00000686515.1:n.2010-162A>G (ATP7A)
ENST00000686543.1:c.1870-162A>G (ATP7A) ENSP00000509477.1:n.1870-162A>G
ENST00000686688.1:c.1870-162A>G (ATP7A) ENSP00000509416.1:n.1870-162A>G
ENST00000686999.1:n.2181-162A>G (ATP7A)
ENST00000687086.1:c.1870-162A>G (ATP7A) ENSP00000509566.1:n.1870-162A>G
ENST00000687628.1:n.3721A>G (ATP7A)
ENST00000688746.1:n.2022-162A>G (ATP7A)
ENST00000689530.1:c.1870-162A>G (ATP7A) ENSP00000509707.1:n.1870-162A>G
ENST00000689649.1:c.1870-162A>G (ATP7A) ENSP00000509277.1:n.1870-162A>G
ENST00000689767.1:c.1963-162A>G (ATP7A) ENSP00000509406.1:n.1963-162A>G
ENST00000689872.1:c.1870-435A>G (ATP7A) ENSP00000509373.1:n.1870-435A>G
ENST00000692110.1:c.1786-162A>G (ATP7A) ENSP00000509366.1:n.1786-162A>G
ENST00000692908.1:c.1870-162A>G (ATP7A) ENSP00000508627.1:n.1870-162A>G
ENST00000693398.1:c.1870-162A>G (ATP7A) ENSP00000510089.1:n.1870-162A>G
ENST00000341514.11:c.1870-162A>G (ATP7A) MANE Select ENSP00000345728.6:n.1870-162A>G
ENST00000644362.1:c.-19-98853A>G (PGK1) ENSP00000496140.1:n.-19-98853A>G
ENST00000645094.1:c.*1784-162A>G (ATP7A) ENSP00000493605.1:n.*1784-162A>G
ENST00000341514.10:c.1870-162A>G (ATP7A) ENSP00000345728.6:n.1870-162A>G
ENST00000343533.9:c.1870-162A>G (ATP7A) ENSP00000343026.5:n.1870-162A>G
ENST00000350425.5:c.*1043-162A>G (ATP7A) ENSP00000343678.5:n.*1043-162A>G
NM_000052.6:c.1870-162A>G (ATP7A) NP_000043.4:n.1870-162A>G
NM_001282224.1:c.1870-162A>G (ATP7A) NP_001269153.1:n.1870-162A>G
NR_104109.1:n.322-20386A>G (ATP7A)
NM_000052.7:c.1870-162A>G (ATP7A) MANE Select NP_000043.4:n.1870-162A>G
NR_104109.2:n.285-20386A>G (ATP7A)
NM_001282224.2:c.1870-162A>G (ATP7A) NP_001269153.1:n.1870-162A>G