Canonical Allele Identifier: CA413602777

Gene: ATP7A PGK1

Linked Data

• MyVariant Identifiers: chrX:g.77276481T>G (hg19) ; chrX:g.78020984T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.78020984T>G , CM000685.2:g.78020984T>G	GRCh38
NC_000023.10:g.77276481T>G , CM000685.1:g.77276481T>G	GRCh37
NC_000023.9:g.77163137T>G	NCBI36
NG_013224.2:g.115288T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000343533.10:c.2851T>G (ATP7A)	ENSP00000343026.6:p.Phe951Val
ENST00000682475.1:n.1238T>G (ATP7A)
ENST00000685033.1:c.375+586T>G (ATP7A)	ENSP00000509269.1:n.375+586T>G
ENST00000685264.1:c.2821T>G (ATP7A)	ENSP00000510136.1:p.Phe941Val
ENST00000686033.1:c.2821T>G (ATP7A)	ENSP00000510693.1:p.Phe941Val
ENST00000686133.1:c.2821T>G (ATP7A)	ENSP00000509233.1:p.Phe941Val
ENST00000686255.1:n.1852T>G (ATP7A)
ENST00000686543.1:c.2587T>G (ATP7A)	ENSP00000509477.1:p.Phe863Val
ENST00000687086.1:c.2821T>G (ATP7A)	ENSP00000509566.1:p.Phe941Val
ENST00000689514.1:n.863T>G (ATP7A)
ENST00000689530.1:c.2821T>G (ATP7A)	ENSP00000509707.1:p.Phe941Val
ENST00000689767.1:c.2914T>G (ATP7A)	ENSP00000509406.1:p.Phe972Val
ENST00000692908.1:c.2587T>G (ATP7A)	ENSP00000508627.1:p.Phe863Val
ENST00000341514.11:c.2821T>G (ATP7A) MANE Select	ENSP00000345728.6:p.Phe941Val
ENST00000644362.1:c.-19-88883T>G (PGK1)	ENSP00000496140.1:n.-19-88883T>G
ENST00000645094.1:c.*2735T>G (ATP7A)	ENSP00000493605.1:n.*2735T>G
ENST00000341514.10:c.2821T>G (ATP7A)	ENSP00000345728.6:p.Phe941Val
ENST00000343533.9:c.2587T>G (ATP7A)	ENSP00000343026.5:p.Phe863Val
ENST00000350425.5:c.*1994T>G (ATP7A)	ENSP00000343678.5:n.*1994T>G
NM_000052.6:c.2821T>G (ATP7A)	NP_000043.4:p.Phe941Val
NM_001282224.1:c.2587T>G (ATP7A)	NP_001269153.1:p.Phe863Val
NR_104109.1:n.322-10416T>G (ATP7A)
NM_000052.7:c.2821T>G (ATP7A) MANE Select	NP_000043.4:p.Phe941Val
NR_104109.2:n.285-10416T>G (ATP7A)
NM_001282224.2:c.2587T>G (ATP7A)	NP_001269153.1:p.Phe863Val