Canonical Allele Identifier: CA517074038

Gene: ATP7A PGK1

Linked Data

• MyVariant Identifiers: chrX:g.77289219A>T (hg19)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343533.10:c.3441A>T (ATP7A)	ENSP00000343026.6:p.Ile1147=
ENST00000682475.1:n.1828A>T (ATP7A)
ENST00000685033.1:c.675A>T (ATP7A)	ENSP00000509269.1:p.Ile225=
ENST00000685264.1:c.3411A>T (ATP7A)	ENSP00000510136.1:p.Ile1137=
ENST00000686033.1:c.3216A>T (ATP7A)	ENSP00000510693.1:p.Ile1072=
ENST00000686133.1:c.3411A>T (ATP7A)	ENSP00000509233.1:p.Ile1137=
ENST00000686255.1:n.2442A>T (ATP7A)
ENST00000686543.1:c.3177A>T (ATP7A)	ENSP00000509477.1:p.Ile1059=
ENST00000687086.1:c.3411A>T (ATP7A)	ENSP00000509566.1:p.Ile1137=
ENST00000689514.1:n.1453A>T (ATP7A)
ENST00000689767.1:c.3504A>T (ATP7A)	ENSP00000509406.1:p.Ile1168=
ENST00000692908.1:c.3177A>T (ATP7A)	ENSP00000508627.1:p.Ile1059=
ENST00000341514.11:c.3411A>T (ATP7A) MANE Select	ENSP00000345728.6:p.Ile1137=
ENST00000644362.1:c.-19-76146A>T (PGK1)	ENSP00000496140.1:n.-19-76146A>T
ENST00000645094.1:c.*3325A>T (ATP7A)	ENSP00000493605.1:n.*3325A>T
ENST00000341514.10:c.3411A>T (ATP7A)	ENSP00000345728.6:p.Ile1137=
ENST00000343533.9:c.3177A>T (ATP7A)	ENSP00000343026.5:p.Ile1059=
ENST00000350425.5:c.*2584A>T (ATP7A)	ENSP00000343678.5:n.*2584A>T
NM_000052.6:c.3411A>T (ATP7A)	NP_000043.4:p.Ile1137=
NM_001282224.1:c.3177A>T (ATP7A)	NP_001269153.1:p.Ile1059=
NR_104109.1:n.621A>T (ATP7A)
NM_000052.7:c.3411A>T (ATP7A) MANE Select	NP_000043.4:p.Ile1137=
NR_104109.2:n.584A>T (ATP7A)
NM_001282224.2:c.3177A>T (ATP7A)	NP_001269153.1:p.Ile1059=