Canonical Allele Identifier: CA517460803

Linked Data

MyVariant Identifiers: chrX:g.77267129T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.78011632T>C , CM000685.2:g.78011632T>C GRCh38
NC_000023.10:g.77267129T>C , CM000685.1:g.77267129T>C GRCh37
NC_000023.9:g.77153785T>C NCBI36
NG_013224.2:g.105936T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000343533.10:c.2160T>C (ATP7A) ENSP00000343026.6:p.Ser720=
ENST00000682475.1:n.781T>C (ATP7A)
ENST00000685264.1:c.2130T>C (ATP7A) ENSP00000510136.1:p.Ser710=
ENST00000686033.1:c.2130T>C (ATP7A) ENSP00000510693.1:p.Ser710=
ENST00000686133.1:c.2130T>C (ATP7A) ENSP00000509233.1:p.Ser710=
ENST00000686255.1:n.1161T>C (ATP7A)
ENST00000686480.1:c.2130T>C (ATP7A) ENSP00000508978.1:p.Ser710=
ENST00000686515.1:n.2270T>C (ATP7A)
ENST00000686543.1:c.2130T>C (ATP7A) ENSP00000509477.1:p.Ser710=
ENST00000686688.1:c.2130T>C (ATP7A) ENSP00000509416.1:p.Ser710=
ENST00000686999.1:n.2441T>C (ATP7A)
ENST00000687086.1:c.2130T>C (ATP7A) ENSP00000509566.1:p.Ser710=
ENST00000687628.1:n.4339T>C (ATP7A)
ENST00000688746.1:n.2282T>C (ATP7A)
ENST00000689514.1:n.172T>C (ATP7A)
ENST00000689530.1:c.2130T>C (ATP7A) ENSP00000509707.1:p.Ser710=
ENST00000689649.1:c.2130T>C (ATP7A) ENSP00000509277.1:p.Ser710=
ENST00000689767.1:c.2223T>C (ATP7A) ENSP00000509406.1:p.Ser741=
ENST00000689872.1:c.*79T>C (ATP7A) ENSP00000509373.1:n.*79T>C
ENST00000692110.1:c.2046T>C (ATP7A) ENSP00000509366.1:p.Ser682=
ENST00000692908.1:c.2130T>C (ATP7A) ENSP00000508627.1:p.Ser710=
ENST00000693398.1:c.2130T>C (ATP7A) ENSP00000510089.1:p.Ser710=
ENST00000341514.11:c.2130T>C (ATP7A) MANE Select ENSP00000345728.6:p.Ser710=
ENST00000644362.1:c.-19-98235T>C (PGK1) ENSP00000496140.1:n.-19-98235T>C
ENST00000645094.1:c.*2044T>C (ATP7A) ENSP00000493605.1:n.*2044T>C
ENST00000341514.10:c.2130T>C (ATP7A) ENSP00000345728.6:p.Ser710=
ENST00000343533.9:c.2130T>C (ATP7A) ENSP00000343026.5:p.Ser710=
ENST00000350425.5:c.*1303T>C (ATP7A) ENSP00000343678.5:n.*1303T>C
NM_000052.6:c.2130T>C (ATP7A) NP_000043.4:p.Ser710=
NM_001282224.1:c.2130T>C (ATP7A) NP_001269153.1:p.Ser710=
NR_104109.1:n.322-19768T>C (ATP7A)
NM_000052.7:c.2130T>C (ATP7A) MANE Select NP_000043.4:p.Ser710=
NR_104109.2:n.285-19768T>C (ATP7A)
NM_001282224.2:c.2130T>C (ATP7A) NP_001269153.1:p.Ser710=