Canonical Allele Identifier: CA207468

Gene: ATP7A PGK1

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.78014707A>G , CM000685.2:g.78014707A>G	GRCh38
NC_000023.10:g.77270204A>G , CM000685.1:g.77270204A>G	GRCh37
NC_000023.9:g.77156860A>G	NCBI36
NG_013224.2:g.109011A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343533.10:c.2482A>G (ATP7A)	ENSP00000343026.6:p.Thr828Ala
ENST00000682475.1:n.869A>G (ATP7A)
ENST00000685033.1:c.46A>G (ATP7A)	ENSP00000509269.1:p.Thr16Ala
ENST00000685264.1:c.2452A>G (ATP7A)	ENSP00000510136.1:p.Thr818Ala
ENST00000686033.1:c.2452A>G (ATP7A)	ENSP00000510693.1:p.Thr818Ala
ENST00000686133.1:c.2452A>G (ATP7A)	ENSP00000509233.1:p.Thr818Ala
ENST00000686255.1:n.1483A>G (ATP7A)
ENST00000686480.1:c.2218A>G (ATP7A)	ENSP00000508978.1:p.Thr740Ala
ENST00000686543.1:c.2218A>G (ATP7A)	ENSP00000509477.1:p.Thr740Ala
ENST00000686688.1:c.2452A>G (ATP7A)	ENSP00000509416.1:p.Thr818Ala
ENST00000687086.1:c.2452A>G (ATP7A)	ENSP00000509566.1:p.Thr818Ala
ENST00000689514.1:n.494A>G (ATP7A)
ENST00000689530.1:c.2452A>G (ATP7A)	ENSP00000509707.1:p.Thr818Ala
ENST00000689649.1:c.2452A>G (ATP7A)	ENSP00000509277.1:p.Thr818Ala
ENST00000689767.1:c.2545A>G (ATP7A)	ENSP00000509406.1:p.Thr849Ala
ENST00000689872.1:c.*401A>G (ATP7A)	ENSP00000509373.1:n.*401A>G
ENST00000692908.1:c.2218A>G (ATP7A)	ENSP00000508627.1:p.Thr740Ala
ENST00000693398.1:c.2452A>G (ATP7A)	ENSP00000510089.1:p.Thr818Ala
ENST00000341514.11:c.2452A>G (ATP7A) MANE Select	ENSP00000345728.6:p.Thr818Ala
ENST00000644362.1:c.-19-95160A>G (PGK1)	ENSP00000496140.1:n.-19-95160A>G
ENST00000645094.1:c.*2366A>G (ATP7A)	ENSP00000493605.1:n.*2366A>G
ENST00000341514.10:c.2452A>G (ATP7A)	ENSP00000345728.6:p.Thr818Ala
ENST00000343533.9:c.2218A>G (ATP7A)	ENSP00000343026.5:p.Thr740Ala
ENST00000350425.5:c.*1625A>G (ATP7A)	ENSP00000343678.5:n.*1625A>G
NM_000052.6:c.2452A>G (ATP7A)	NP_000043.4:p.Thr818Ala
NM_001282224.1:c.2218A>G (ATP7A)	NP_001269153.1:p.Thr740Ala
NR_104109.1:n.322-16693A>G (ATP7A)
NM_000052.7:c.2452A>G (ATP7A) MANE Select	NP_000043.4:p.Thr818Ala
NR_104109.2:n.285-16693A>G (ATP7A)
NM_001282224.2:c.2218A>G (ATP7A)	NP_001269153.1:p.Thr740Ala