Canonical Allele Identifier: CA517064786

Gene: ATP7A PGK1

Linked Data

• MyVariant Identifiers: chrX:g.77276477C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.78020980C>A , CM000685.2:g.78020980C>A	GRCh38
NC_000023.10:g.77276477C>A , CM000685.1:g.77276477C>A	GRCh37
NC_000023.9:g.77163133C>A	NCBI36
NG_013224.2:g.115284C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343533.10:c.2847C>A (ATP7A)	ENSP00000343026.6:p.Gly949=
ENST00000682475.1:n.1234C>A (ATP7A)
ENST00000685033.1:c.375+582C>A (ATP7A)	ENSP00000509269.1:n.375+582C>A
ENST00000685264.1:c.2817C>A (ATP7A)	ENSP00000510136.1:p.Gly939=
ENST00000686033.1:c.2817C>A (ATP7A)	ENSP00000510693.1:p.Gly939=
ENST00000686133.1:c.2817C>A (ATP7A)	ENSP00000509233.1:p.Gly939=
ENST00000686255.1:n.1848C>A (ATP7A)
ENST00000686543.1:c.2583C>A (ATP7A)	ENSP00000509477.1:p.Gly861=
ENST00000687086.1:c.2817C>A (ATP7A)	ENSP00000509566.1:p.Gly939=
ENST00000689514.1:n.859C>A (ATP7A)
ENST00000689530.1:c.2817C>A (ATP7A)	ENSP00000509707.1:p.Gly939=
ENST00000689767.1:c.2910C>A (ATP7A)	ENSP00000509406.1:p.Gly970=
ENST00000692908.1:c.2583C>A (ATP7A)	ENSP00000508627.1:p.Gly861=
ENST00000341514.11:c.2817C>A (ATP7A) MANE Select	ENSP00000345728.6:p.Gly939=
ENST00000644362.1:c.-19-88887C>A (PGK1)	ENSP00000496140.1:n.-19-88887C>A
ENST00000645094.1:c.*2731C>A (ATP7A)	ENSP00000493605.1:n.*2731C>A
ENST00000341514.10:c.2817C>A (ATP7A)	ENSP00000345728.6:p.Gly939=
ENST00000343533.9:c.2583C>A (ATP7A)	ENSP00000343026.5:p.Gly861=
ENST00000350425.5:c.*1990C>A (ATP7A)	ENSP00000343678.5:n.*1990C>A
NM_000052.6:c.2817C>A (ATP7A)	NP_000043.4:p.Gly939=
NM_001282224.1:c.2583C>A (ATP7A)	NP_001269153.1:p.Gly861=
NR_104109.1:n.322-10420C>A (ATP7A)
NM_000052.7:c.2817C>A (ATP7A) MANE Select	NP_000043.4:p.Gly939=
NR_104109.2:n.285-10420C>A (ATP7A)
NM_001282224.2:c.2583C>A (ATP7A)	NP_001269153.1:p.Gly861=