Canonical Allele Identifier: CA2439099610

Gene: ATP7A PGK1

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.78009207C= , CM000685.2:g.78009207C=	GRCh38
NC_000023.10:g.77264704C= , CM000685.1:g.77264704C=	GRCh37
NC_000023.9:g.77151360C=	NCBI36
NG_013224.2:g.103511C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343533.10:c.1843C= (ATP7A)	ENSP00000343026.6:p.His615=
ENST00000682742.2:n.1975C= (ATP7A)
ENST00000685264.1:c.1813C= (ATP7A)	ENSP00000510136.1:p.His605=
ENST00000685434.1:n.1847C= (ATP7A)
ENST00000686033.1:c.1813C= (ATP7A)	ENSP00000510693.1:p.His605=
ENST00000686133.1:c.1813C= (ATP7A)	ENSP00000509233.1:p.His605=
ENST00000686416.1:n.2167C= (ATP7A)
ENST00000686480.1:c.1813C= (ATP7A)	ENSP00000508978.1:p.His605=
ENST00000686515.1:n.1953C= (ATP7A)
ENST00000686543.1:c.1813C= (ATP7A)	ENSP00000509477.1:p.His605=
ENST00000686688.1:c.1813C= (ATP7A)	ENSP00000509416.1:p.His605=
ENST00000686999.1:n.2124C= (ATP7A)
ENST00000687086.1:c.1813C= (ATP7A)	ENSP00000509566.1:p.His605=
ENST00000687628.1:n.1914C= (ATP7A)
ENST00000688746.1:n.1965C= (ATP7A)
ENST00000689530.1:c.1813C= (ATP7A)	ENSP00000509707.1:p.His605=
ENST00000689541.1:n.2122C= (ATP7A)
ENST00000689649.1:c.1813C= (ATP7A)	ENSP00000509277.1:p.His605=
ENST00000689767.1:c.1906C= (ATP7A)	ENSP00000509406.1:p.His636=
ENST00000689872.1:c.1813C= (ATP7A)	ENSP00000509373.1:p.His605=
ENST00000692110.1:c.1729C= (ATP7A)	ENSP00000509366.1:p.His577=
ENST00000692908.1:c.1813C= (ATP7A)	ENSP00000508627.1:p.His605=
ENST00000693387.1:c.*1742C= (ATP7A)	ENSP00000508732.1:n.*1742C=
ENST00000693398.1:c.1813C= (ATP7A)	ENSP00000510089.1:p.His605=
ENST00000341514.11:c.1813C= (ATP7A) MANE Select	ENSP00000345728.6:p.His605=
ENST00000644362.1:c.-20+98372C= (PGK1)	ENSP00000496140.1:n.-20+98372C=
ENST00000645094.1:c.*1727C= (ATP7A)	ENSP00000493605.1:n.*1727C=
ENST00000341514.10:c.1813C= (ATP7A)	ENSP00000345728.6:p.His605=
ENST00000343533.9:c.1813C= (ATP7A)	ENSP00000343026.5:p.His605=
ENST00000350425.5:c.*986C= (ATP7A)	ENSP00000343678.5:n.*986C=
NM_000052.6:c.1813C= (ATP7A)	NP_000043.4:p.His605=
NM_001282224.1:c.1813C= (ATP7A)	NP_001269153.1:p.His605=
NR_104109.1:n.322-22193C= (ATP7A)
NM_000052.7:c.1813C= (ATP7A) MANE Select	NP_000043.4:p.His605=
NR_104109.2:n.285-22193C= (ATP7A)
NM_001282224.2:c.1813C= (ATP7A)	NP_001269153.1:p.His605=