Canonical Allele Identifier: CA413599636

Gene: ATP7A PGK1

Linked Data

• MyVariant Identifiers: chrX:g.77268598C>G (hg19) ; chrX:g.78013101C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.78013101C>G , CM000685.2:g.78013101C>G	GRCh38
NC_000023.10:g.77268598C>G , CM000685.1:g.77268598C>G	GRCh37
NC_000023.9:g.77155254C>G	NCBI36
NG_013224.2:g.107405C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343533.10:c.2425C>G (ATP7A)	ENSP00000343026.6:p.His809Asp
ENST00000682475.1:n.823+1427C>G (ATP7A)
ENST00000685264.1:c.2395C>G (ATP7A)	ENSP00000510136.1:p.His799Asp
ENST00000686033.1:c.2395C>G (ATP7A)	ENSP00000510693.1:p.His799Asp
ENST00000686133.1:c.2395C>G (ATP7A)	ENSP00000509233.1:p.His799Asp
ENST00000686255.1:n.1426C>G (ATP7A)
ENST00000686480.1:c.2172+1427C>G (ATP7A)	ENSP00000508978.1:n.2172+1427C>G
ENST00000686543.1:c.2172+1427C>G (ATP7A)	ENSP00000509477.1:n.2172+1427C>G
ENST00000686688.1:c.2395C>G (ATP7A)	ENSP00000509416.1:p.His799Asp
ENST00000687086.1:c.2395C>G (ATP7A)	ENSP00000509566.1:p.His799Asp
ENST00000688746.1:n.3751C>G (ATP7A)
ENST00000689514.1:n.437C>G (ATP7A)
ENST00000689530.1:c.2395C>G (ATP7A)	ENSP00000509707.1:p.His799Asp
ENST00000689649.1:c.2395C>G (ATP7A)	ENSP00000509277.1:p.His799Asp
ENST00000689767.1:c.2488C>G (ATP7A)	ENSP00000509406.1:p.His830Asp
ENST00000689872.1:c.*344C>G (ATP7A)	ENSP00000509373.1:n.*344C>G
ENST00000692908.1:c.2172+1427C>G (ATP7A)	ENSP00000508627.1:n.2172+1427C>G
ENST00000693398.1:c.2395C>G (ATP7A)	ENSP00000510089.1:p.His799Asp
ENST00000341514.11:c.2395C>G (ATP7A) MANE Select	ENSP00000345728.6:p.His799Asp
ENST00000644362.1:c.-19-96766C>G (PGK1)	ENSP00000496140.1:n.-19-96766C>G
ENST00000645094.1:c.*2309C>G (ATP7A)	ENSP00000493605.1:n.*2309C>G
ENST00000341514.10:c.2395C>G (ATP7A)	ENSP00000345728.6:p.His799Asp
ENST00000343533.9:c.2172+1427C>G (ATP7A)	ENSP00000343026.5:n.2172+1427C>G
ENST00000350425.5:c.*1568C>G (ATP7A)	ENSP00000343678.5:n.*1568C>G
NM_000052.6:c.2395C>G (ATP7A)	NP_000043.4:p.His799Asp
NM_001282224.1:c.2172+1427C>G (ATP7A)	NP_001269153.1:n.2172+1427C>G
NR_104109.1:n.322-18299C>G (ATP7A)
NM_000052.7:c.2395C>G (ATP7A) MANE Select	NP_000043.4:p.His799Asp
NR_104109.2:n.285-18299C>G (ATP7A)
NM_001282224.2:c.2172+1427C>G (ATP7A)	NP_001269153.1:n.2172+1427C>G