Linked Data
ClinVar Variation Id:
1653959
ClinVar RCV Id:
RCV002163595
dbSNP Id:
rs782037158
gnomAD v2:
X-77267141-G-A
gnomAD v3:
X-78011644-G-A
gnomAD v4:
X-78011644-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.78011644G>A , CM000685.2:g.78011644G>A | GRCh38 |
| NC_000023.10:g.77267141G>A , CM000685.1:g.77267141G>A | GRCh37 |
| NC_000023.9:g.77153797G>A | NCBI36 |
| NG_013224.2:g.105948G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000343533.10:c.2172G>A (ATP7A) | ENSP00000343026.6:p.Leu724= | |
| ENST00000682475.1:n.793G>A (ATP7A) | ||
| ENST00000685264.1:c.2142G>A (ATP7A) | ENSP00000510136.1:p.Leu714= | |
| ENST00000686033.1:c.2142G>A (ATP7A) | ENSP00000510693.1:p.Leu714= | |
| ENST00000686133.1:c.2142G>A (ATP7A) | ENSP00000509233.1:p.Leu714= | |
| ENST00000686255.1:n.1173G>A (ATP7A) | ||
| ENST00000686480.1:c.2142G>A (ATP7A) | ENSP00000508978.1:p.Leu714= | |
| ENST00000686515.1:n.2282G>A (ATP7A) | ||
| ENST00000686543.1:c.2142G>A (ATP7A) | ENSP00000509477.1:p.Leu714= | |
| ENST00000686688.1:c.2142G>A (ATP7A) | ENSP00000509416.1:p.Leu714= | |
| ENST00000686999.1:n.2453G>A (ATP7A) | ||
| ENST00000687086.1:c.2142G>A (ATP7A) | ENSP00000509566.1:p.Leu714= | |
| ENST00000687628.1:n.4351G>A (ATP7A) | ||
| ENST00000688746.1:n.2294G>A (ATP7A) | ||
| ENST00000689514.1:n.184G>A (ATP7A) | ||
| ENST00000689530.1:c.2142G>A (ATP7A) | ENSP00000509707.1:p.Leu714= | |
| ENST00000689649.1:c.2142G>A (ATP7A) | ENSP00000509277.1:p.Leu714= | |
| ENST00000689767.1:c.2235G>A (ATP7A) | ENSP00000509406.1:p.Leu745= | |
| ENST00000689872.1:c.*91G>A (ATP7A) | ENSP00000509373.1:n.*91G>A | |
| ENST00000692110.1:c.2058G>A (ATP7A) | ENSP00000509366.1:p.Leu686= | |
| ENST00000692908.1:c.2142G>A (ATP7A) | ENSP00000508627.1:p.Leu714= | |
| ENST00000693398.1:c.2142G>A (ATP7A) | ENSP00000510089.1:p.Leu714= | |
| ENST00000341514.11:c.2142G>A (ATP7A) MANE Select | ENSP00000345728.6:p.Leu714= | |
| ENST00000644362.1:c.-19-98223G>A (PGK1) | ENSP00000496140.1:n.-19-98223G>A | |
| ENST00000645094.1:c.*2056G>A (ATP7A) | ENSP00000493605.1:n.*2056G>A | |
| ENST00000341514.10:c.2142G>A (ATP7A) | ENSP00000345728.6:p.Leu714= | |
| ENST00000343533.9:c.2142G>A (ATP7A) | ENSP00000343026.5:p.Leu714= | |
| ENST00000350425.5:c.*1315G>A (ATP7A) | ENSP00000343678.5:n.*1315G>A | |
| NM_000052.6:c.2142G>A (ATP7A) | NP_000043.4:p.Leu714= | |
| NM_001282224.1:c.2142G>A (ATP7A) | NP_001269153.1:p.Leu714= | |
| NR_104109.1:n.322-19756G>A (ATP7A) | ||
| NM_000052.7:c.2142G>A (ATP7A) MANE Select | NP_000043.4:p.Leu714= | |
| NR_104109.2:n.285-19756G>A (ATP7A) | ||
| NM_001282224.2:c.2142G>A (ATP7A) | NP_001269153.1:p.Leu714= |