Canonical Allele Identifier: CA413599662

Gene: ATP7A PGK1

Linked Data

• ClinVar Variation Id: 2945466
• ClinVar RCV Id: RCV003803560
• dbSNP Id: rs1557234761
• gnomAD v2: X-77268604-G-A
• gnomAD v4: X-78013107-G-A
• MyVariant Identifiers: chrX:g.77268604G>A (hg19) ; chrX:g.78013107G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.78013107G>A , CM000685.2:g.78013107G>A	GRCh38
NC_000023.10:g.77268604G>A , CM000685.1:g.77268604G>A	GRCh37
NC_000023.9:g.77155260G>A	NCBI36
NG_013224.2:g.107411G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000343533.10:c.2431G>A (ATP7A)	ENSP00000343026.6:p.Ala811Thr
ENST00000682475.1:n.823+1433G>A (ATP7A)
ENST00000685264.1:c.2401G>A (ATP7A)	ENSP00000510136.1:p.Ala801Thr
ENST00000686033.1:c.2401G>A (ATP7A)	ENSP00000510693.1:p.Ala801Thr
ENST00000686133.1:c.2401G>A (ATP7A)	ENSP00000509233.1:p.Ala801Thr
ENST00000686255.1:n.1432G>A (ATP7A)
ENST00000686480.1:c.2172+1433G>A (ATP7A)	ENSP00000508978.1:n.2172+1433G>A
ENST00000686543.1:c.2172+1433G>A (ATP7A)	ENSP00000509477.1:n.2172+1433G>A
ENST00000686688.1:c.2401G>A (ATP7A)	ENSP00000509416.1:p.Ala801Thr
ENST00000687086.1:c.2401G>A (ATP7A)	ENSP00000509566.1:p.Ala801Thr
ENST00000688746.1:n.3757G>A (ATP7A)
ENST00000689514.1:n.443G>A (ATP7A)
ENST00000689530.1:c.2401G>A (ATP7A)	ENSP00000509707.1:p.Ala801Thr
ENST00000689649.1:c.2401G>A (ATP7A)	ENSP00000509277.1:p.Ala801Thr
ENST00000689767.1:c.2494G>A (ATP7A)	ENSP00000509406.1:p.Ala832Thr
ENST00000689872.1:c.*350G>A (ATP7A)	ENSP00000509373.1:n.*350G>A
ENST00000692908.1:c.2172+1433G>A (ATP7A)	ENSP00000508627.1:n.2172+1433G>A
ENST00000693398.1:c.2401G>A (ATP7A)	ENSP00000510089.1:p.Ala801Thr
ENST00000341514.11:c.2401G>A (ATP7A) MANE Select	ENSP00000345728.6:p.Ala801Thr
ENST00000644362.1:c.-19-96760G>A (PGK1)	ENSP00000496140.1:n.-19-96760G>A
ENST00000645094.1:c.*2315G>A (ATP7A)	ENSP00000493605.1:n.*2315G>A
ENST00000341514.10:c.2401G>A (ATP7A)	ENSP00000345728.6:p.Ala801Thr
ENST00000343533.9:c.2172+1433G>A (ATP7A)	ENSP00000343026.5:n.2172+1433G>A
ENST00000350425.5:c.*1574G>A (ATP7A)	ENSP00000343678.5:n.*1574G>A
NM_000052.6:c.2401G>A (ATP7A)	NP_000043.4:p.Ala801Thr
NM_001282224.1:c.2172+1433G>A (ATP7A)	NP_001269153.1:n.2172+1433G>A
NR_104109.1:n.322-18293G>A (ATP7A)
NM_000052.7:c.2401G>A (ATP7A) MANE Select	NP_000043.4:p.Ala801Thr
NR_104109.2:n.285-18293G>A (ATP7A)
NM_001282224.2:c.2172+1433G>A (ATP7A)	NP_001269153.1:n.2172+1433G>A