Canonical Allele Identifier: CA413597018

Gene: ATP7A PGK1

Linked Data

• MyVariant Identifiers: chrX:g.77264651C>A (hg19) ; chrX:g.78009154C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.78009154C>A , CM000685.2:g.78009154C>A	GRCh38
NC_000023.10:g.77264651C>A , CM000685.1:g.77264651C>A	GRCh37
NC_000023.9:g.77151307C>A	NCBI36
NG_013224.2:g.103458C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343533.10:c.1790C>A (ATP7A)	ENSP00000343026.6:p.Thr597Lys
ENST00000682742.2:n.1922C>A (ATP7A)
ENST00000685264.1:c.1760C>A (ATP7A)	ENSP00000510136.1:p.Thr587Lys
ENST00000685434.1:n.1794C>A (ATP7A)
ENST00000686033.1:c.1760C>A (ATP7A)	ENSP00000510693.1:p.Thr587Lys
ENST00000686133.1:c.1760C>A (ATP7A)	ENSP00000509233.1:p.Thr587Lys
ENST00000686416.1:n.2114C>A (ATP7A)
ENST00000686480.1:c.1760C>A (ATP7A)	ENSP00000508978.1:p.Thr587Lys
ENST00000686515.1:n.1900C>A (ATP7A)
ENST00000686543.1:c.1760C>A (ATP7A)	ENSP00000509477.1:p.Thr587Lys
ENST00000686688.1:c.1760C>A (ATP7A)	ENSP00000509416.1:p.Thr587Lys
ENST00000686999.1:n.2071C>A (ATP7A)
ENST00000687086.1:c.1760C>A (ATP7A)	ENSP00000509566.1:p.Thr587Lys
ENST00000687628.1:n.1861C>A (ATP7A)
ENST00000688746.1:n.1912C>A (ATP7A)
ENST00000689530.1:c.1760C>A (ATP7A)	ENSP00000509707.1:p.Thr587Lys
ENST00000689541.1:n.2069C>A (ATP7A)
ENST00000689649.1:c.1760C>A (ATP7A)	ENSP00000509277.1:p.Thr587Lys
ENST00000689767.1:c.1853C>A (ATP7A)	ENSP00000509406.1:p.Thr618Lys
ENST00000689872.1:c.1760C>A (ATP7A)	ENSP00000509373.1:p.Thr587Lys
ENST00000692110.1:c.1676C>A (ATP7A)	ENSP00000509366.1:p.Thr559Lys
ENST00000692908.1:c.1760C>A (ATP7A)	ENSP00000508627.1:p.Thr587Lys
ENST00000693387.1:c.*1689C>A (ATP7A)	ENSP00000508732.1:n.*1689C>A
ENST00000693398.1:c.1760C>A (ATP7A)	ENSP00000510089.1:p.Thr587Lys
ENST00000341514.11:c.1760C>A (ATP7A) MANE Select	ENSP00000345728.6:p.Thr587Lys
ENST00000644362.1:c.-20+98319C>A (PGK1)	ENSP00000496140.1:n.-20+98319C>A
ENST00000645094.1:c.*1674C>A (ATP7A)	ENSP00000493605.1:n.*1674C>A
ENST00000341514.10:c.1760C>A (ATP7A)	ENSP00000345728.6:p.Thr587Lys
ENST00000343533.9:c.1760C>A (ATP7A)	ENSP00000343026.5:p.Thr587Lys
ENST00000350425.5:c.*933C>A (ATP7A)	ENSP00000343678.5:n.*933C>A
NM_000052.6:c.1760C>A (ATP7A)	NP_000043.4:p.Thr587Lys
NM_001282224.1:c.1760C>A (ATP7A)	NP_001269153.1:p.Thr587Lys
NR_104109.1:n.322-22246C>A (ATP7A)
NM_000052.7:c.1760C>A (ATP7A) MANE Select	NP_000043.4:p.Thr587Lys
NR_104109.2:n.285-22246C>A (ATP7A)
NM_001282224.2:c.1760C>A (ATP7A)	NP_001269153.1:p.Thr587Lys