Canonical Allele Identifier: CA517460620

Linked Data

MyVariant Identifiers: chrX:g.77266958T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.78011461T>A , CM000685.2:g.78011461T>A GRCh38
NC_000023.10:g.77266958T>A , CM000685.1:g.77266958T>A GRCh37
NC_000023.9:g.77153614T>A NCBI36
NG_013224.2:g.105765T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000343533.10:c.1989T>A (ATP7A) ENSP00000343026.6:p.Ser663=
ENST00000682475.1:n.610T>A (ATP7A)
ENST00000685264.1:c.1959T>A (ATP7A) ENSP00000510136.1:p.Ser653=
ENST00000686033.1:c.1959T>A (ATP7A) ENSP00000510693.1:p.Ser653=
ENST00000686133.1:c.1959T>A (ATP7A) ENSP00000509233.1:p.Ser653=
ENST00000686255.1:n.990T>A (ATP7A)
ENST00000686480.1:c.1959T>A (ATP7A) ENSP00000508978.1:p.Ser653=
ENST00000686515.1:n.2099T>A (ATP7A)
ENST00000686543.1:c.1959T>A (ATP7A) ENSP00000509477.1:p.Ser653=
ENST00000686688.1:c.1959T>A (ATP7A) ENSP00000509416.1:p.Ser653=
ENST00000686999.1:n.2270T>A (ATP7A)
ENST00000687086.1:c.1959T>A (ATP7A) ENSP00000509566.1:p.Ser653=
ENST00000687628.1:n.4168T>A (ATP7A)
ENST00000688746.1:n.2111T>A (ATP7A)
ENST00000689514.1:n.1T>A (ATP7A)
ENST00000689530.1:c.1959T>A (ATP7A) ENSP00000509707.1:p.Ser653=
ENST00000689649.1:c.1959T>A (ATP7A) ENSP00000509277.1:p.Ser653=
ENST00000689767.1:c.2052T>A (ATP7A) ENSP00000509406.1:p.Ser684=
ENST00000689872.1:c.1882T>A (ATP7A) ENSP00000509373.1:p.Phe628Ile
ENST00000692110.1:c.1875T>A (ATP7A) ENSP00000509366.1:p.Ser625=
ENST00000692908.1:c.1959T>A (ATP7A) ENSP00000508627.1:p.Ser653=
ENST00000693398.1:c.1959T>A (ATP7A) ENSP00000510089.1:p.Ser653=
ENST00000341514.11:c.1959T>A (ATP7A) MANE Select ENSP00000345728.6:p.Ser653=
ENST00000644362.1:c.-19-98406T>A (PGK1) ENSP00000496140.1:n.-19-98406T>A
ENST00000645094.1:c.*1873T>A (ATP7A) ENSP00000493605.1:n.*1873T>A
ENST00000341514.10:c.1959T>A (ATP7A) ENSP00000345728.6:p.Ser653=
ENST00000343533.9:c.1959T>A (ATP7A) ENSP00000343026.5:p.Ser653=
ENST00000350425.5:c.*1132T>A (ATP7A) ENSP00000343678.5:n.*1132T>A
NM_000052.6:c.1959T>A (ATP7A) NP_000043.4:p.Ser653=
NM_001282224.1:c.1959T>A (ATP7A) NP_001269153.1:p.Ser653=
NR_104109.1:n.322-19939T>A (ATP7A)
NM_000052.7:c.1959T>A (ATP7A) MANE Select NP_000043.4:p.Ser653=
NR_104109.2:n.285-19939T>A (ATP7A)
NM_001282224.2:c.1959T>A (ATP7A) NP_001269153.1:p.Ser653=