Canonical Allele Identifier: CA277066
Gene: ATP7A HGNC NCBI
PGK1 HGNC NCBI

Linked Data

ClinVar Variation Id: 210420
ClinVar RCV Id: RCV000193058
dbSNP Id: rs797045350
MyVariant Identifiers: chrX:g.77268386G>A (hg19) chrX:g.78012889G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.78012889G>A , CM000685.2:g.78012889G>A GRCh38
NC_000023.10:g.77268386G>A , CM000685.1:g.77268386G>A GRCh37
NC_000023.9:g.77155042G>A NCBI36
NG_013224.2:g.107193G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000343533.10:c.2213G>A (ATP7A) ENSP00000343026.6:p.Gly738Asp
ENST00000682475.1:n.823+1215G>A (ATP7A)
ENST00000685264.1:c.2183G>A (ATP7A) ENSP00000510136.1:p.Gly728Asp
ENST00000686033.1:c.2183G>A (ATP7A) ENSP00000510693.1:p.Gly728Asp
ENST00000686133.1:c.2183G>A (ATP7A) ENSP00000509233.1:p.Gly728Asp
ENST00000686255.1:n.1214G>A (ATP7A)
ENST00000686480.1:c.2172+1215G>A (ATP7A) ENSP00000508978.1:n.2172+1215G>A
ENST00000686543.1:c.2172+1215G>A (ATP7A) ENSP00000509477.1:n.2172+1215G>A
ENST00000686688.1:c.2183G>A (ATP7A) ENSP00000509416.1:p.Gly728Asp
ENST00000687086.1:c.2183G>A (ATP7A) ENSP00000509566.1:p.Gly728Asp
ENST00000688746.1:n.3539G>A (ATP7A)
ENST00000689514.1:n.225G>A (ATP7A)
ENST00000689530.1:c.2183G>A (ATP7A) ENSP00000509707.1:p.Gly728Asp
ENST00000689649.1:c.2183G>A (ATP7A) ENSP00000509277.1:p.Gly728Asp
ENST00000689767.1:c.2276G>A (ATP7A) ENSP00000509406.1:p.Gly759Asp
ENST00000689872.1:c.*132G>A (ATP7A) ENSP00000509373.1:n.*132G>A
ENST00000692908.1:c.2172+1215G>A (ATP7A) ENSP00000508627.1:n.2172+1215G>A
ENST00000693398.1:c.2183G>A (ATP7A) ENSP00000510089.1:p.Gly728Asp
ENST00000341514.11:c.2183G>A (ATP7A) MANE Select ENSP00000345728.6:p.Gly728Asp
ENST00000644362.1:c.-19-96978G>A (PGK1) ENSP00000496140.1:n.-19-96978G>A
ENST00000645094.1:c.*2097G>A (ATP7A) ENSP00000493605.1:n.*2097G>A
ENST00000341514.10:c.2183G>A (ATP7A) ENSP00000345728.6:p.Gly728Asp
ENST00000343533.9:c.2172+1215G>A (ATP7A) ENSP00000343026.5:n.2172+1215G>A
ENST00000350425.5:c.*1356G>A (ATP7A) ENSP00000343678.5:n.*1356G>A
NM_000052.6:c.2183G>A (ATP7A) NP_000043.4:p.Gly728Asp
NM_001282224.1:c.2172+1215G>A (ATP7A) NP_001269153.1:n.2172+1215G>A
NR_104109.1:n.322-18511G>A (ATP7A)
NM_000052.7:c.2183G>A (ATP7A) MANE Select NP_000043.4:p.Gly728Asp
NR_104109.2:n.285-18511G>A (ATP7A)
NM_001282224.2:c.2172+1215G>A (ATP7A) NP_001269153.1:n.2172+1215G>A
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