Canonical Allele Identifier: CA2439099603

Gene: ATP7A PGK1

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.78009187C= , CM000685.2:g.78009187C=	GRCh38
NC_000023.10:g.77264684C= , CM000685.1:g.77264684C=	GRCh37
NC_000023.9:g.77151340C=	NCBI36
NG_013224.2:g.103491C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343533.10:c.1823C= (ATP7A)	ENSP00000343026.6:p.Ala608=
ENST00000682742.2:n.1955C= (ATP7A)
ENST00000685264.1:c.1793C= (ATP7A)	ENSP00000510136.1:p.Ala598=
ENST00000685434.1:n.1827C= (ATP7A)
ENST00000686033.1:c.1793C= (ATP7A)	ENSP00000510693.1:p.Ala598=
ENST00000686133.1:c.1793C= (ATP7A)	ENSP00000509233.1:p.Ala598=
ENST00000686416.1:n.2147C= (ATP7A)
ENST00000686480.1:c.1793C= (ATP7A)	ENSP00000508978.1:p.Ala598=
ENST00000686515.1:n.1933C= (ATP7A)
ENST00000686543.1:c.1793C= (ATP7A)	ENSP00000509477.1:p.Ala598=
ENST00000686688.1:c.1793C= (ATP7A)	ENSP00000509416.1:p.Ala598=
ENST00000686999.1:n.2104C= (ATP7A)
ENST00000687086.1:c.1793C= (ATP7A)	ENSP00000509566.1:p.Ala598=
ENST00000687628.1:n.1894C= (ATP7A)
ENST00000688746.1:n.1945C= (ATP7A)
ENST00000689530.1:c.1793C= (ATP7A)	ENSP00000509707.1:p.Ala598=
ENST00000689541.1:n.2102C= (ATP7A)
ENST00000689649.1:c.1793C= (ATP7A)	ENSP00000509277.1:p.Ala598=
ENST00000689767.1:c.1886C= (ATP7A)	ENSP00000509406.1:p.Ala629=
ENST00000689872.1:c.1793C= (ATP7A)	ENSP00000509373.1:p.Ala598=
ENST00000692110.1:c.1709C= (ATP7A)	ENSP00000509366.1:p.Ala570=
ENST00000692908.1:c.1793C= (ATP7A)	ENSP00000508627.1:p.Ala598=
ENST00000693387.1:c.*1722C= (ATP7A)	ENSP00000508732.1:n.*1722C=
ENST00000693398.1:c.1793C= (ATP7A)	ENSP00000510089.1:p.Ala598=
ENST00000341514.11:c.1793C= (ATP7A) MANE Select	ENSP00000345728.6:p.Ala598=
ENST00000644362.1:c.-20+98352C= (PGK1)	ENSP00000496140.1:n.-20+98352C=
ENST00000645094.1:c.*1707C= (ATP7A)	ENSP00000493605.1:n.*1707C=
ENST00000341514.10:c.1793C= (ATP7A)	ENSP00000345728.6:p.Ala598=
ENST00000343533.9:c.1793C= (ATP7A)	ENSP00000343026.5:p.Ala598=
ENST00000350425.5:c.*966C= (ATP7A)	ENSP00000343678.5:n.*966C=
NM_000052.6:c.1793C= (ATP7A)	NP_000043.4:p.Ala598=
NM_001282224.1:c.1793C= (ATP7A)	NP_001269153.1:p.Ala598=
NR_104109.1:n.322-22213C= (ATP7A)
NM_000052.7:c.1793C= (ATP7A) MANE Select	NP_000043.4:p.Ala598=
NR_104109.2:n.285-22213C= (ATP7A)
NM_001282224.2:c.1793C= (ATP7A)	NP_001269153.1:p.Ala598=