Canonical Allele Identifier: CA517064568

Gene: ATP7A PGK1

Linked Data

• MyVariant Identifiers: chrX:g.77276444T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.78020947T>G , CM000685.2:g.78020947T>G	GRCh38
NC_000023.10:g.77276444T>G , CM000685.1:g.77276444T>G	GRCh37
NC_000023.9:g.77163100T>G	NCBI36
NG_013224.2:g.115251T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343533.10:c.2814T>G (ATP7A)	ENSP00000343026.6:p.Ala938=
ENST00000682475.1:n.1201T>G (ATP7A)
ENST00000685033.1:c.375+549T>G (ATP7A)	ENSP00000509269.1:n.375+549T>G
ENST00000685264.1:c.2784T>G (ATP7A)	ENSP00000510136.1:p.Ala928=
ENST00000686033.1:c.2784T>G (ATP7A)	ENSP00000510693.1:p.Ala928=
ENST00000686133.1:c.2784T>G (ATP7A)	ENSP00000509233.1:p.Ala928=
ENST00000686255.1:n.1815T>G (ATP7A)
ENST00000686543.1:c.2550T>G (ATP7A)	ENSP00000509477.1:p.Ala850=
ENST00000687086.1:c.2784T>G (ATP7A)	ENSP00000509566.1:p.Ala928=
ENST00000689514.1:n.826T>G (ATP7A)
ENST00000689530.1:c.2784T>G (ATP7A)	ENSP00000509707.1:p.Ala928=
ENST00000689767.1:c.2877T>G (ATP7A)	ENSP00000509406.1:p.Ala959=
ENST00000692908.1:c.2550T>G (ATP7A)	ENSP00000508627.1:p.Ala850=
ENST00000341514.11:c.2784T>G (ATP7A) MANE Select	ENSP00000345728.6:p.Ala928=
ENST00000644362.1:c.-19-88920T>G (PGK1)	ENSP00000496140.1:n.-19-88920T>G
ENST00000645094.1:c.*2698T>G (ATP7A)	ENSP00000493605.1:n.*2698T>G
ENST00000341514.10:c.2784T>G (ATP7A)	ENSP00000345728.6:p.Ala928=
ENST00000343533.9:c.2550T>G (ATP7A)	ENSP00000343026.5:p.Ala850=
ENST00000350425.5:c.*1957T>G (ATP7A)	ENSP00000343678.5:n.*1957T>G
NM_000052.6:c.2784T>G (ATP7A)	NP_000043.4:p.Ala928=
NM_001282224.1:c.2550T>G (ATP7A)	NP_001269153.1:p.Ala850=
NR_104109.1:n.322-10453T>G (ATP7A)
NM_000052.7:c.2784T>G (ATP7A) MANE Select	NP_000043.4:p.Ala928=
NR_104109.2:n.285-10453T>G (ATP7A)
NM_001282224.2:c.2550T>G (ATP7A)	NP_001269153.1:p.Ala850=