Canonical Allele Identifier: CA413604102

Gene: ATP7A PGK1

Linked Data

• MyVariant Identifiers: chrX:g.77289219A>G (hg19) ; chrX:g.78033721A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.78033721A>G , CM000685.2:g.78033721A>G	GRCh38
NC_000023.10:g.77289219A>G , CM000685.1:g.77289219A>G	GRCh37
NC_000023.9:g.77175875A>G	NCBI36
NG_013224.2:g.128025A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343533.10:c.3441A>G (ATP7A)	ENSP00000343026.6:p.Ile1147Met
ENST00000682475.1:n.1828A>G (ATP7A)
ENST00000685033.1:c.675A>G (ATP7A)	ENSP00000509269.1:p.Ile225Met
ENST00000685264.1:c.3411A>G (ATP7A)	ENSP00000510136.1:p.Ile1137Met
ENST00000686033.1:c.3216A>G (ATP7A)	ENSP00000510693.1:p.Ile1072Met
ENST00000686133.1:c.3411A>G (ATP7A)	ENSP00000509233.1:p.Ile1137Met
ENST00000686255.1:n.2442A>G (ATP7A)
ENST00000686543.1:c.3177A>G (ATP7A)	ENSP00000509477.1:p.Ile1059Met
ENST00000687086.1:c.3411A>G (ATP7A)	ENSP00000509566.1:p.Ile1137Met
ENST00000689514.1:n.1453A>G (ATP7A)
ENST00000689767.1:c.3504A>G (ATP7A)	ENSP00000509406.1:p.Ile1168Met
ENST00000692908.1:c.3177A>G (ATP7A)	ENSP00000508627.1:p.Ile1059Met
ENST00000341514.11:c.3411A>G (ATP7A) MANE Select	ENSP00000345728.6:p.Ile1137Met
ENST00000644362.1:c.-19-76146A>G (PGK1)	ENSP00000496140.1:n.-19-76146A>G
ENST00000645094.1:c.*3325A>G (ATP7A)	ENSP00000493605.1:n.*3325A>G
ENST00000341514.10:c.3411A>G (ATP7A)	ENSP00000345728.6:p.Ile1137Met
ENST00000343533.9:c.3177A>G (ATP7A)	ENSP00000343026.5:p.Ile1059Met
ENST00000350425.5:c.*2584A>G (ATP7A)	ENSP00000343678.5:n.*2584A>G
NM_000052.6:c.3411A>G (ATP7A)	NP_000043.4:p.Ile1137Met
NM_001282224.1:c.3177A>G (ATP7A)	NP_001269153.1:p.Ile1059Met
NR_104109.1:n.621A>G (ATP7A)
NM_000052.7:c.3411A>G (ATP7A) MANE Select	NP_000043.4:p.Ile1137Met
NR_104109.2:n.584A>G (ATP7A)
NM_001282224.2:c.3177A>G (ATP7A)	NP_001269153.1:p.Ile1059Met