Canonical Allele Identifier: CA2499226890

Gene: ATP7A PGK1

Linked Data

• ClinVar Variation Id: 1095519
• ClinVar RCV Id: RCV001416420
• dbSNP Id: rs2149107266

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.78033830A>T , CM000685.2:g.78033830A>T	GRCh38
NC_000023.10:g.77289328A>T , CM000685.1:g.77289328A>T	GRCh37
NC_000023.9:g.77175984A>T	NCBI36
NG_013224.2:g.128134A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343533.10:c.3541+9A>T (ATP7A)	ENSP00000343026.6:n.3541+9A>T
ENST00000682475.1:n.1928+9A>T (ATP7A)
ENST00000685033.1:c.775+9A>T (ATP7A)	ENSP00000509269.1:n.775+9A>T
ENST00000685264.1:c.3511+9A>T (ATP7A)	ENSP00000510136.1:n.3511+9A>T
ENST00000686033.1:c.3316+9A>T (ATP7A)	ENSP00000510693.1:n.3316+9A>T
ENST00000686133.1:c.3511+9A>T (ATP7A)	ENSP00000509233.1:n.3511+9A>T
ENST00000686255.1:n.2542+9A>T (ATP7A)
ENST00000686543.1:c.3277+9A>T (ATP7A)	ENSP00000509477.1:n.3277+9A>T
ENST00000687086.1:c.3511+9A>T (ATP7A)	ENSP00000509566.1:n.3511+9A>T
ENST00000689514.1:n.1553+9A>T (ATP7A)
ENST00000689767.1:c.3604+9A>T (ATP7A)	ENSP00000509406.1:n.3604+9A>T
ENST00000692908.1:c.3277+9A>T (ATP7A)	ENSP00000508627.1:n.3277+9A>T
ENST00000341514.11:c.3511+9A>T (ATP7A) MANE Select	ENSP00000345728.6:n.3511+9A>T
ENST00000644362.1:c.-19-76037A>T (PGK1)	ENSP00000496140.1:n.-19-76037A>T
ENST00000645094.1:c.*3425+9A>T (ATP7A)	ENSP00000493605.1:n.*3425+9A>T
ENST00000341514.10:c.3511+9A>T (ATP7A)	ENSP00000345728.6:n.3511+9A>T
ENST00000343533.9:c.3277+9A>T (ATP7A)	ENSP00000343026.5:n.3277+9A>T
ENST00000350425.5:c.*2684+9A>T (ATP7A)	ENSP00000343678.5:n.*2684+9A>T
NM_000052.6:c.3511+9A>T (ATP7A)	NP_000043.4:n.3511+9A>T
NM_001282224.1:c.3277+9A>T (ATP7A)	NP_001269153.1:n.3277+9A>T
NR_104109.1:n.721+9A>T (ATP7A)
NM_000052.7:c.3511+9A>T (ATP7A) MANE Select	NP_000043.4:n.3511+9A>T
NR_104109.2:n.684+9A>T (ATP7A)
NM_001282224.2:c.3277+9A>T (ATP7A)	NP_001269153.1:n.3277+9A>T