Canonical Allele Identifier: CA413602925

Gene: ATP7A PGK1

Linked Data

• gnomAD v4: X-78021054-T-C
• MyVariant Identifiers: chrX:g.77276551T>C (hg19) ; chrX:g.78021054T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.78021054T>C , CM000685.2:g.78021054T>C	GRCh38
NC_000023.10:g.77276551T>C , CM000685.1:g.77276551T>C	GRCh37
NC_000023.9:g.77163207T>C	NCBI36
NG_013224.2:g.115358T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343533.10:c.2921T>C (ATP7A)	ENSP00000343026.6:p.Phe974Ser
ENST00000682475.1:n.1308T>C (ATP7A)
ENST00000685033.1:c.375+656T>C (ATP7A)	ENSP00000509269.1:n.375+656T>C
ENST00000685264.1:c.2891T>C (ATP7A)	ENSP00000510136.1:p.Phe964Ser
ENST00000686033.1:c.2891T>C (ATP7A)	ENSP00000510693.1:p.Phe964Ser
ENST00000686133.1:c.2891T>C (ATP7A)	ENSP00000509233.1:p.Phe964Ser
ENST00000686255.1:n.1922T>C (ATP7A)
ENST00000686543.1:c.2657T>C (ATP7A)	ENSP00000509477.1:p.Phe886Ser
ENST00000687086.1:c.2891T>C (ATP7A)	ENSP00000509566.1:p.Phe964Ser
ENST00000689514.1:n.933T>C (ATP7A)
ENST00000689530.1:c.2891T>C (ATP7A)	ENSP00000509707.1:p.Phe964Ser
ENST00000689767.1:c.2984T>C (ATP7A)	ENSP00000509406.1:p.Phe995Ser
ENST00000692908.1:c.2657T>C (ATP7A)	ENSP00000508627.1:p.Phe886Ser
ENST00000341514.11:c.2891T>C (ATP7A) MANE Select	ENSP00000345728.6:p.Phe964Ser
ENST00000644362.1:c.-19-88813T>C (PGK1)	ENSP00000496140.1:n.-19-88813T>C
ENST00000645094.1:c.*2805T>C (ATP7A)	ENSP00000493605.1:n.*2805T>C
ENST00000341514.10:c.2891T>C (ATP7A)	ENSP00000345728.6:p.Phe964Ser
ENST00000343533.9:c.2657T>C (ATP7A)	ENSP00000343026.5:p.Phe886Ser
ENST00000350425.5:c.*2064T>C (ATP7A)	ENSP00000343678.5:n.*2064T>C
NM_000052.6:c.2891T>C (ATP7A)	NP_000043.4:p.Phe964Ser
NM_001282224.1:c.2657T>C (ATP7A)	NP_001269153.1:p.Phe886Ser
NR_104109.1:n.322-10346T>C (ATP7A)
NM_000052.7:c.2891T>C (ATP7A) MANE Select	NP_000043.4:p.Phe964Ser
NR_104109.2:n.285-10346T>C (ATP7A)
NM_001282224.2:c.2657T>C (ATP7A)	NP_001269153.1:p.Phe886Ser