Linked Data
dbSNP Id:
rs782487449
ExAC:
X:77266645 A / G
gnomAD v2:
X-77266645-A-G
gnomAD v3:
X-78011148-A-G
gnomAD v4:
X-78011148-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.78011148A>G , CM000685.2:g.78011148A>G | GRCh38 |
| NC_000023.10:g.77266645A>G , CM000685.1:g.77266645A>G | GRCh37 |
| NC_000023.9:g.77153301A>G | NCBI36 |
| NG_013224.2:g.105452A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000343533.10:c.1900-28A>G (ATP7A) | ENSP00000343026.6:n.1900-28A>G | |
| ENST00000682475.1:n.297A>G (ATP7A) | ||
| ENST00000685264.1:c.1870-28A>G (ATP7A) | ENSP00000510136.1:n.1870-28A>G | |
| ENST00000686033.1:c.1870-28A>G (ATP7A) | ENSP00000510693.1:n.1870-28A>G | |
| ENST00000686133.1:c.1870-28A>G (ATP7A) | ENSP00000509233.1:n.1870-28A>G | |
| ENST00000686255.1:n.677A>G (ATP7A) | ||
| ENST00000686480.1:c.1870-28A>G (ATP7A) | ENSP00000508978.1:n.1870-28A>G | |
| ENST00000686515.1:n.2010-28A>G (ATP7A) | ||
| ENST00000686543.1:c.1870-28A>G (ATP7A) | ENSP00000509477.1:n.1870-28A>G | |
| ENST00000686688.1:c.1870-28A>G (ATP7A) | ENSP00000509416.1:n.1870-28A>G | |
| ENST00000686999.1:n.2181-28A>G (ATP7A) | ||
| ENST00000687086.1:c.1870-28A>G (ATP7A) | ENSP00000509566.1:n.1870-28A>G | |
| ENST00000687628.1:n.3855A>G (ATP7A) | ||
| ENST00000688746.1:n.2022-28A>G (ATP7A) | ||
| ENST00000689530.1:c.1870-28A>G (ATP7A) | ENSP00000509707.1:n.1870-28A>G | |
| ENST00000689649.1:c.1870-28A>G (ATP7A) | ENSP00000509277.1:n.1870-28A>G | |
| ENST00000689767.1:c.1963-28A>G (ATP7A) | ENSP00000509406.1:n.1963-28A>G | |
| ENST00000689872.1:c.1870-301A>G (ATP7A) | ENSP00000509373.1:n.1870-301A>G | |
| ENST00000692110.1:c.1786-28A>G (ATP7A) | ENSP00000509366.1:n.1786-28A>G | |
| ENST00000692908.1:c.1870-28A>G (ATP7A) | ENSP00000508627.1:n.1870-28A>G | |
| ENST00000693398.1:c.1870-28A>G (ATP7A) | ENSP00000510089.1:n.1870-28A>G | |
| ENST00000341514.11:c.1870-28A>G (ATP7A) MANE Select | ENSP00000345728.6:n.1870-28A>G | |
| ENST00000644362.1:c.-19-98719A>G (PGK1) | ENSP00000496140.1:n.-19-98719A>G | |
| ENST00000645094.1:c.*1784-28A>G (ATP7A) | ENSP00000493605.1:n.*1784-28A>G | |
| ENST00000341514.10:c.1870-28A>G (ATP7A) | ENSP00000345728.6:n.1870-28A>G | |
| ENST00000343533.9:c.1870-28A>G (ATP7A) | ENSP00000343026.5:n.1870-28A>G | |
| ENST00000350425.5:c.*1043-28A>G (ATP7A) | ENSP00000343678.5:n.*1043-28A>G | |
| NM_000052.6:c.1870-28A>G (ATP7A) | NP_000043.4:n.1870-28A>G | |
| NM_001282224.1:c.1870-28A>G (ATP7A) | NP_001269153.1:n.1870-28A>G | |
| NR_104109.1:n.322-20252A>G (ATP7A) | ||
| NM_000052.7:c.1870-28A>G (ATP7A) MANE Select | NP_000043.4:n.1870-28A>G | |
| NR_104109.2:n.285-20252A>G (ATP7A) | ||
| NM_001282224.2:c.1870-28A>G (ATP7A) | NP_001269153.1:n.1870-28A>G |