Canonical Allele Identifier: CA413599221

Gene: ATP7A PGK1

Linked Data

• MyVariant Identifiers: chrX:g.77268519A>T (hg19) ; chrX:g.78013022A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.78013022A>T , CM000685.2:g.78013022A>T	GRCh38
NC_000023.10:g.77268519A>T , CM000685.1:g.77268519A>T	GRCh37
NC_000023.9:g.77155175A>T	NCBI36
NG_013224.2:g.107326A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343533.10:c.2346A>T (ATP7A)	ENSP00000343026.6:p.Arg782Ser
ENST00000682475.1:n.823+1348A>T (ATP7A)
ENST00000685264.1:c.2316A>T (ATP7A)	ENSP00000510136.1:p.Arg772Ser
ENST00000686033.1:c.2316A>T (ATP7A)	ENSP00000510693.1:p.Arg772Ser
ENST00000686133.1:c.2316A>T (ATP7A)	ENSP00000509233.1:p.Arg772Ser
ENST00000686255.1:n.1347A>T (ATP7A)
ENST00000686480.1:c.2172+1348A>T (ATP7A)	ENSP00000508978.1:n.2172+1348A>T
ENST00000686543.1:c.2172+1348A>T (ATP7A)	ENSP00000509477.1:n.2172+1348A>T
ENST00000686688.1:c.2316A>T (ATP7A)	ENSP00000509416.1:p.Arg772Ser
ENST00000687086.1:c.2316A>T (ATP7A)	ENSP00000509566.1:p.Arg772Ser
ENST00000688746.1:n.3672A>T (ATP7A)
ENST00000689514.1:n.358A>T (ATP7A)
ENST00000689530.1:c.2316A>T (ATP7A)	ENSP00000509707.1:p.Arg772Ser
ENST00000689649.1:c.2316A>T (ATP7A)	ENSP00000509277.1:p.Arg772Ser
ENST00000689767.1:c.2409A>T (ATP7A)	ENSP00000509406.1:p.Arg803Ser
ENST00000689872.1:c.*265A>T (ATP7A)	ENSP00000509373.1:n.*265A>T
ENST00000692908.1:c.2172+1348A>T (ATP7A)	ENSP00000508627.1:n.2172+1348A>T
ENST00000693398.1:c.2316A>T (ATP7A)	ENSP00000510089.1:p.Arg772Ser
ENST00000341514.11:c.2316A>T (ATP7A) MANE Select	ENSP00000345728.6:p.Arg772Ser
ENST00000644362.1:c.-19-96845A>T (PGK1)	ENSP00000496140.1:n.-19-96845A>T
ENST00000645094.1:c.*2230A>T (ATP7A)	ENSP00000493605.1:n.*2230A>T
ENST00000341514.10:c.2316A>T (ATP7A)	ENSP00000345728.6:p.Arg772Ser
ENST00000343533.9:c.2172+1348A>T (ATP7A)	ENSP00000343026.5:n.2172+1348A>T
ENST00000350425.5:c.*1489A>T (ATP7A)	ENSP00000343678.5:n.*1489A>T
NM_000052.6:c.2316A>T (ATP7A)	NP_000043.4:p.Arg772Ser
NM_001282224.1:c.2172+1348A>T (ATP7A)	NP_001269153.1:n.2172+1348A>T
NR_104109.1:n.322-18378A>T (ATP7A)
NM_000052.7:c.2316A>T (ATP7A) MANE Select	NP_000043.4:p.Arg772Ser
NR_104109.2:n.285-18378A>T (ATP7A)
NM_001282224.2:c.2172+1348A>T (ATP7A)	NP_001269153.1:n.2172+1348A>T