Revel Score:
ENST00000343533
0.494
ENST00000341514 (MANE Select)
0.494
ENST00000355691
0.494
ClinVar RCV:
ClinVar Variation:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.77989546A>G , CM000685.2:g.77989546A>G | GRCh38 |
| NC_000023.10:g.77245042A>G , CM000685.1:g.77245042A>G | GRCh37 |
| NC_000023.9:g.77131698A>G | NCBI36 |
| NG_013224.2:g.83850A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000343533.10:c.954A>G (ATP7A) | ENSP00000343026.6:p.Ile318Met | |
| ENST00000682742.2:n.1086A>G (ATP7A) | ||
| ENST00000685208.1:n.1587A>G (ATP7A) | ||
| ENST00000685264.1:c.924A>G (ATP7A) | ENSP00000510136.1:p.Ile308Met | |
| ENST00000685434.1:n.1042A>G (ATP7A) | ||
| ENST00000685885.1:c.960A>G (ATP7A) | ENSP00000510005.1:p.Ile320Met | |
| ENST00000686033.1:c.924A>G (ATP7A) | ENSP00000510693.1:p.Ile308Met | |
| ENST00000686133.1:c.924A>G (ATP7A) | ENSP00000509233.1:p.Ile308Met | |
| ENST00000686416.1:n.1278A>G (ATP7A) | ||
| ENST00000686480.1:c.924A>G (ATP7A) | ENSP00000508978.1:p.Ile308Met | |
| ENST00000686515.1:n.1064A>G (ATP7A) | ||
| ENST00000686543.1:c.924A>G (ATP7A) | ENSP00000509477.1:p.Ile308Met | |
| ENST00000686688.1:c.924A>G (ATP7A) | ENSP00000509416.1:p.Ile308Met | |
| ENST00000686999.1:n.1235A>G (ATP7A) | ||
| ENST00000687086.1:c.924A>G (ATP7A) | ENSP00000509566.1:p.Ile308Met | |
| ENST00000687416.1:c.924A>G (ATP7A) | ENSP00000510310.1:p.Ile308Met | |
| ENST00000687599.1:c.924A>G (ATP7A) | ENSP00000508745.1:p.Ile308Met | |
| ENST00000687628.1:n.1025A>G (ATP7A) | ||
| ENST00000687984.1:c.924A>G (ATP7A) | ENSP00000510772.1:p.Ile308Met | |
| ENST00000688249.1:c.924A>G (ATP7A) | ENSP00000510644.1:p.Ile308Met | |
| ENST00000688338.1:c.924A>G (ATP7A) | ENSP00000508672.1:p.Ile308Met | |
| ENST00000688746.1:n.1076A>G (ATP7A) | ||
| ENST00000688889.1:c.*838A>G (ATP7A) | ENSP00000508610.1:n.*838A>G | |
| ENST00000689530.1:c.924A>G (ATP7A) | ENSP00000509707.1:p.Ile308Met | |
| ENST00000689541.1:n.1233A>G (ATP7A) | ||
| ENST00000689649.1:c.924A>G (ATP7A) | ENSP00000509277.1:p.Ile308Met | |
| ENST00000689767.1:c.924A>G (ATP7A) | ENSP00000509406.1:p.Ile308Met | |
| ENST00000689872.1:c.924A>G (ATP7A) | ENSP00000509373.1:p.Ile308Met | |
| ENST00000689891.1:c.924A>G (ATP7A) | ENSP00000508974.1:p.Ile308Met | |
| ENST00000691152.1:c.924A>G (ATP7A) | ENSP00000508843.1:p.Ile308Met | |
| ENST00000691456.1:n.1215A>G (ATP7A) | ||
| ENST00000692110.1:c.924A>G (ATP7A) | ENSP00000509366.1:p.Ile308Met | |
| ENST00000692908.1:c.924A>G (ATP7A) | ENSP00000508627.1:p.Ile308Met | |
| ENST00000693051.1:c.924A>G (ATP7A) | ENSP00000510332.1:p.Ile308Met | |
| ENST00000693387.1:c.*853A>G (ATP7A) | ENSP00000508732.1:n.*853A>G | |
| ENST00000693398.1:c.924A>G (ATP7A) | ENSP00000510089.1:p.Ile308Met | |
| ENST00000341514.11:c.924A>G (ATP7A) MANE Select | ENSP00000345728.6:p.Ile308Met | |
| ENST00000644362.1:c.-20+78711A>G (PGK1) | ENSP00000496140.1:n.-20+78711A>G | |
| ENST00000645094.1:c.*838A>G (ATP7A) | ENSP00000493605.1:n.*838A>G | |
| ENST00000341514.10:c.924A>G (ATP7A) | ENSP00000345728.6:p.Ile308Met | |
| ENST00000343533.9:c.924A>G (ATP7A) | ENSP00000343026.5:p.Ile308Met | |
| ENST00000350425.5:c.*97A>G (ATP7A) | ENSP00000343678.5:n.*97A>G | |
| NM_000052.6:c.924A>G (ATP7A) | NP_000043.4:p.Ile308Met | |
| NM_001282224.1:c.924A>G (ATP7A) | NP_001269153.1:p.Ile308Met | |
| NR_104109.1:n.321+17785A>G (ATP7A) | ||
| NM_000052.7:c.924A>G (ATP7A) MANE Select | NP_000043.4:p.Ile308Met | |
| NR_104109.2:n.284+17785A>G (ATP7A) | ||
| NM_001282224.2:c.924A>G (ATP7A) | NP_001269153.1:p.Ile308Met |