Canonical Allele Identifier: CA413599540

Gene: ATP7A PGK1

Linked Data

• MyVariant Identifiers: chrX:g.77268577G>C (hg19) ; chrX:g.78013080G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.78013080G>C , CM000685.2:g.78013080G>C	GRCh38
NC_000023.10:g.77268577G>C , CM000685.1:g.77268577G>C	GRCh37
NC_000023.9:g.77155233G>C	NCBI36
NG_013224.2:g.107384G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343533.10:c.2404G>C (ATP7A)	ENSP00000343026.6:p.Ala802Pro
ENST00000682475.1:n.823+1406G>C (ATP7A)
ENST00000685264.1:c.2374G>C (ATP7A)	ENSP00000510136.1:p.Ala792Pro
ENST00000686033.1:c.2374G>C (ATP7A)	ENSP00000510693.1:p.Ala792Pro
ENST00000686133.1:c.2374G>C (ATP7A)	ENSP00000509233.1:p.Ala792Pro
ENST00000686255.1:n.1405G>C (ATP7A)
ENST00000686480.1:c.2172+1406G>C (ATP7A)	ENSP00000508978.1:n.2172+1406G>C
ENST00000686543.1:c.2172+1406G>C (ATP7A)	ENSP00000509477.1:n.2172+1406G>C
ENST00000686688.1:c.2374G>C (ATP7A)	ENSP00000509416.1:p.Ala792Pro
ENST00000687086.1:c.2374G>C (ATP7A)	ENSP00000509566.1:p.Ala792Pro
ENST00000688746.1:n.3730G>C (ATP7A)
ENST00000689514.1:n.416G>C (ATP7A)
ENST00000689530.1:c.2374G>C (ATP7A)	ENSP00000509707.1:p.Ala792Pro
ENST00000689649.1:c.2374G>C (ATP7A)	ENSP00000509277.1:p.Ala792Pro
ENST00000689767.1:c.2467G>C (ATP7A)	ENSP00000509406.1:p.Ala823Pro
ENST00000689872.1:c.*323G>C (ATP7A)	ENSP00000509373.1:n.*323G>C
ENST00000692908.1:c.2172+1406G>C (ATP7A)	ENSP00000508627.1:n.2172+1406G>C
ENST00000693398.1:c.2374G>C (ATP7A)	ENSP00000510089.1:p.Ala792Pro
ENST00000341514.11:c.2374G>C (ATP7A) MANE Select	ENSP00000345728.6:p.Ala792Pro
ENST00000644362.1:c.-19-96787G>C (PGK1)	ENSP00000496140.1:n.-19-96787G>C
ENST00000645094.1:c.*2288G>C (ATP7A)	ENSP00000493605.1:n.*2288G>C
ENST00000341514.10:c.2374G>C (ATP7A)	ENSP00000345728.6:p.Ala792Pro
ENST00000343533.9:c.2172+1406G>C (ATP7A)	ENSP00000343026.5:n.2172+1406G>C
ENST00000350425.5:c.*1547G>C (ATP7A)	ENSP00000343678.5:n.*1547G>C
NM_000052.6:c.2374G>C (ATP7A)	NP_000043.4:p.Ala792Pro
NM_001282224.1:c.2172+1406G>C (ATP7A)	NP_001269153.1:n.2172+1406G>C
NR_104109.1:n.322-18320G>C (ATP7A)
NM_000052.7:c.2374G>C (ATP7A) MANE Select	NP_000043.4:p.Ala792Pro
NR_104109.2:n.285-18320G>C (ATP7A)
NM_001282224.2:c.2172+1406G>C (ATP7A)	NP_001269153.1:n.2172+1406G>C