Canonical Allele Identifier: CA277319

Linked Data

ClinVar Variation Id: 210408
ClinVar RCV Id: RCV000194429
dbSNP Id: rs797045342

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.78011452G>A , CM000685.2:g.78011452G>A GRCh38
NC_000023.10:g.77266949G>A , CM000685.1:g.77266949G>A GRCh37
NC_000023.9:g.77153605G>A NCBI36
NG_013224.2:g.105756G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000343533.10:c.1980G>A (ATP7A) ENSP00000343026.6:p.Trp660Ter
ENST00000682475.1:n.601G>A (ATP7A)
ENST00000685264.1:c.1950G>A (ATP7A) ENSP00000510136.1:p.Trp650Ter
ENST00000686033.1:c.1950G>A (ATP7A) ENSP00000510693.1:p.Trp650Ter
ENST00000686133.1:c.1950G>A (ATP7A) ENSP00000509233.1:p.Trp650Ter
ENST00000686255.1:n.981G>A (ATP7A)
ENST00000686480.1:c.1950G>A (ATP7A) ENSP00000508978.1:p.Trp650Ter
ENST00000686515.1:n.2090G>A (ATP7A)
ENST00000686543.1:c.1950G>A (ATP7A) ENSP00000509477.1:p.Trp650Ter
ENST00000686688.1:c.1950G>A (ATP7A) ENSP00000509416.1:p.Trp650Ter
ENST00000686999.1:n.2261G>A (ATP7A)
ENST00000687086.1:c.1950G>A (ATP7A) ENSP00000509566.1:p.Trp650Ter
ENST00000687628.1:n.4159G>A (ATP7A)
ENST00000688746.1:n.2102G>A (ATP7A)
ENST00000689530.1:c.1950G>A (ATP7A) ENSP00000509707.1:p.Trp650Ter
ENST00000689649.1:c.1950G>A (ATP7A) ENSP00000509277.1:p.Trp650Ter
ENST00000689767.1:c.2043G>A (ATP7A) ENSP00000509406.1:p.Trp681Ter
ENST00000689872.1:c.1873G>A (ATP7A) ENSP00000509373.1:p.Glu625Lys
ENST00000692110.1:c.1866G>A (ATP7A) ENSP00000509366.1:p.Trp622Ter
ENST00000692908.1:c.1950G>A (ATP7A) ENSP00000508627.1:p.Trp650Ter
ENST00000693398.1:c.1950G>A (ATP7A) ENSP00000510089.1:p.Trp650Ter
ENST00000341514.11:c.1950G>A (ATP7A) MANE Select ENSP00000345728.6:p.Trp650Ter
ENST00000644362.1:c.-19-98415G>A (PGK1) ENSP00000496140.1:n.-19-98415G>A
ENST00000645094.1:c.*1864G>A (ATP7A) ENSP00000493605.1:n.*1864G>A
ENST00000341514.10:c.1950G>A (ATP7A) ENSP00000345728.6:p.Trp650Ter
ENST00000343533.9:c.1950G>A (ATP7A) ENSP00000343026.5:p.Trp650Ter
ENST00000350425.5:c.*1123G>A (ATP7A) ENSP00000343678.5:n.*1123G>A
NM_000052.6:c.1950G>A (ATP7A) NP_000043.4:p.Trp650Ter
NM_001282224.1:c.1950G>A (ATP7A) NP_001269153.1:p.Trp650Ter
NR_104109.1:n.322-19948G>A (ATP7A)
NM_000052.7:c.1950G>A (ATP7A) MANE Select NP_000043.4:p.Trp650Ter
NR_104109.2:n.285-19948G>A (ATP7A)
NM_001282224.2:c.1950G>A (ATP7A) NP_001269153.1:p.Trp650Ter