Canonical Allele Identifier: CA413600177

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.77988632G>T , CM000685.2:g.77988632G>T GRCh38
NC_000023.10:g.77244128G>T , CM000685.1:g.77244128G>T GRCh37
NC_000023.9:g.77130784G>T NCBI36
NG_013224.2:g.82936G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000343533.10:c.541G>T (ATP7A) ENSP00000343026.6:p.Val181Phe
ENST00000682742.2:n.673G>T (ATP7A)
ENST00000685208.1:n.673G>T (ATP7A)
ENST00000685264.1:c.511G>T (ATP7A) ENSP00000510136.1:p.Val171Phe
ENST00000685434.1:n.629G>T (ATP7A)
ENST00000685885.1:c.547G>T (ATP7A) ENSP00000510005.1:p.Val183Phe
ENST00000686033.1:c.511G>T (ATP7A) ENSP00000510693.1:p.Val171Phe
ENST00000686133.1:c.511G>T (ATP7A) ENSP00000509233.1:p.Val171Phe
ENST00000686416.1:n.865G>T (ATP7A)
ENST00000686480.1:c.511G>T (ATP7A) ENSP00000508978.1:p.Val171Phe
ENST00000686515.1:n.651G>T (ATP7A)
ENST00000686543.1:c.511G>T (ATP7A) ENSP00000509477.1:p.Val171Phe
ENST00000686688.1:c.511G>T (ATP7A) ENSP00000509416.1:p.Val171Phe
ENST00000686999.1:n.822G>T (ATP7A)
ENST00000687082.1:n.629G>T (ATP7A)
ENST00000687086.1:c.511G>T (ATP7A) ENSP00000509566.1:p.Val171Phe
ENST00000687325.1:n.814G>T (ATP7A)
ENST00000687416.1:c.511G>T (ATP7A) ENSP00000510310.1:p.Val171Phe
ENST00000687599.1:c.511G>T (ATP7A) ENSP00000508745.1:p.Val171Phe
ENST00000687628.1:n.612G>T (ATP7A)
ENST00000687984.1:c.511G>T (ATP7A) ENSP00000510772.1:p.Val171Phe
ENST00000688249.1:c.511G>T (ATP7A) ENSP00000510644.1:p.Val171Phe
ENST00000688338.1:c.511G>T (ATP7A) ENSP00000508672.1:p.Val171Phe
ENST00000688746.1:n.663G>T (ATP7A)
ENST00000688889.1:c.*425G>T (ATP7A) ENSP00000508610.1:n.*425G>T
ENST00000689530.1:c.511G>T (ATP7A) ENSP00000509707.1:p.Val171Phe
ENST00000689541.1:n.820G>T (ATP7A)
ENST00000689649.1:c.511G>T (ATP7A) ENSP00000509277.1:p.Val171Phe
ENST00000689767.1:c.511G>T (ATP7A) ENSP00000509406.1:p.Val171Phe
ENST00000689872.1:c.511G>T (ATP7A) ENSP00000509373.1:p.Val171Phe
ENST00000689891.1:c.511G>T (ATP7A) ENSP00000508974.1:p.Val171Phe
ENST00000691152.1:c.511G>T (ATP7A) ENSP00000508843.1:p.Val171Phe
ENST00000691456.1:n.802G>T (ATP7A)
ENST00000692110.1:c.511G>T (ATP7A) ENSP00000509366.1:p.Val171Phe
ENST00000692908.1:c.511G>T (ATP7A) ENSP00000508627.1:p.Val171Phe
ENST00000693051.1:c.511G>T (ATP7A) ENSP00000510332.1:p.Val171Phe
ENST00000693387.1:c.*440G>T (ATP7A) ENSP00000508732.1:n.*440G>T
ENST00000693398.1:c.511G>T (ATP7A) ENSP00000510089.1:p.Val171Phe
ENST00000341514.11:c.511G>T (ATP7A) MANE Select ENSP00000345728.6:p.Val171Phe
ENST00000644362.1:c.-20+77797G>T (PGK1) ENSP00000496140.1:n.-20+77797G>T
ENST00000645094.1:c.*425G>T (ATP7A) ENSP00000493605.1:n.*425G>T
ENST00000341514.10:c.511G>T (ATP7A) ENSP00000345728.6:p.Val171Phe
ENST00000343533.9:c.511G>T (ATP7A) ENSP00000343026.5:p.Val171Phe
ENST00000350425.5:c.511G>T (ATP7A) ENSP00000343678.5:p.Val171Phe
NM_000052.6:c.511G>T (ATP7A) NP_000043.4:p.Val171Phe
NM_001282224.1:c.511G>T (ATP7A) NP_001269153.1:p.Val171Phe
NR_104109.1:n.321+16871G>T (ATP7A)
NM_000052.7:c.511G>T (ATP7A) MANE Select NP_000043.4:p.Val171Phe
NR_104109.2:n.284+16871G>T (ATP7A)
NM_001282224.2:c.511G>T (ATP7A) NP_001269153.1:p.Val171Phe