Canonical Allele Identifier: CA517056176

Gene: ATP7A PGK1

Linked Data

• ClinVar Variation Id: 1617352
• ClinVar RCV Id: RCV002076536
• dbSNP Id: rs2077719509
• gnomAD v4: X-77998572-A-G
• MyVariant Identifiers: chrX:g.77254069A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77998572A>G , CM000685.2:g.77998572A>G	GRCh38
NC_000023.10:g.77254069A>G , CM000685.1:g.77254069A>G	GRCh37
NC_000023.9:g.77140725A>G	NCBI36
NG_013224.2:g.92876A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343533.10:c.1461A>G (ATP7A)	ENSP00000343026.6:p.Pro487=
ENST00000682742.2:n.1593A>G (ATP7A)
ENST00000685264.1:c.1431A>G (ATP7A)	ENSP00000510136.1:p.Pro477=
ENST00000685434.1:n.1465A>G (ATP7A)
ENST00000686033.1:c.1431A>G (ATP7A)	ENSP00000510693.1:p.Pro477=
ENST00000686133.1:c.1431A>G (ATP7A)	ENSP00000509233.1:p.Pro477=
ENST00000686416.1:n.1785A>G (ATP7A)
ENST00000686480.1:c.1431A>G (ATP7A)	ENSP00000508978.1:p.Pro477=
ENST00000686515.1:n.1571A>G (ATP7A)
ENST00000686543.1:c.1431A>G (ATP7A)	ENSP00000509477.1:p.Pro477=
ENST00000686688.1:c.1431A>G (ATP7A)	ENSP00000509416.1:p.Pro477=
ENST00000686999.1:n.1742A>G (ATP7A)
ENST00000687086.1:c.1431A>G (ATP7A)	ENSP00000509566.1:p.Pro477=
ENST00000687416.1:c.1431A>G (ATP7A)	ENSP00000510310.1:p.Pro477=
ENST00000687628.1:n.1532A>G (ATP7A)
ENST00000688249.1:c.1431A>G (ATP7A)	ENSP00000510644.1:p.Pro477=
ENST00000688338.1:c.1431A>G (ATP7A)	ENSP00000508672.1:p.Pro477=
ENST00000688746.1:n.1583A>G (ATP7A)
ENST00000689530.1:c.1431A>G (ATP7A)	ENSP00000509707.1:p.Pro477=
ENST00000689541.1:n.1740A>G (ATP7A)
ENST00000689649.1:c.1431A>G (ATP7A)	ENSP00000509277.1:p.Pro477=
ENST00000689767.1:c.1431A>G (ATP7A)	ENSP00000509406.1:p.Pro477=
ENST00000689872.1:c.1431A>G (ATP7A)	ENSP00000509373.1:p.Pro477=
ENST00000691456.1:n.1722A>G (ATP7A)
ENST00000692110.1:c.1347A>G (ATP7A)	ENSP00000509366.1:p.Pro449=
ENST00000692908.1:c.1431A>G (ATP7A)	ENSP00000508627.1:p.Pro477=
ENST00000693051.1:c.1431A>G (ATP7A)	ENSP00000510332.1:p.Pro477=
ENST00000693387.1:c.*1360A>G (ATP7A)	ENSP00000508732.1:n.*1360A>G
ENST00000693398.1:c.1431A>G (ATP7A)	ENSP00000510089.1:p.Pro477=
ENST00000341514.11:c.1431A>G (ATP7A) MANE Select	ENSP00000345728.6:p.Pro477=
ENST00000644362.1:c.-20+87737A>G (PGK1)	ENSP00000496140.1:n.-20+87737A>G
ENST00000645094.1:c.*1345A>G (ATP7A)	ENSP00000493605.1:n.*1345A>G
ENST00000341514.10:c.1431A>G (ATP7A)	ENSP00000345728.6:p.Pro477=
ENST00000343533.9:c.1431A>G (ATP7A)	ENSP00000343026.5:p.Pro477=
ENST00000350425.5:c.*604A>G (ATP7A)	ENSP00000343678.5:n.*604A>G
NM_000052.6:c.1431A>G (ATP7A)	NP_000043.4:p.Pro477=
NM_001282224.1:c.1431A>G (ATP7A)	NP_001269153.1:p.Pro477=
NR_104109.1:n.321+26811A>G (ATP7A)
NM_000052.7:c.1431A>G (ATP7A) MANE Select	NP_000043.4:p.Pro477=
NR_104109.2:n.284+26811A>G (ATP7A)
NM_001282224.2:c.1431A>G (ATP7A)	NP_001269153.1:p.Pro477=