Canonical Allele Identifier: CA413604082

Gene: ATP7A PGK1

Linked Data

• dbSNP Id: rs2077996188
• MyVariant Identifiers: chrX:g.77289212G>A (hg19) ; chrX:g.78033714G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.78033714G>A , CM000685.2:g.78033714G>A	GRCh38
NC_000023.10:g.77289212G>A , CM000685.1:g.77289212G>A	GRCh37
NC_000023.9:g.77175868G>A	NCBI36
NG_013224.2:g.128018G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343533.10:c.3434G>A (ATP7A)	ENSP00000343026.6:p.Trp1145Ter
ENST00000682475.1:n.1821G>A (ATP7A)
ENST00000685033.1:c.668G>A (ATP7A)	ENSP00000509269.1:p.Trp223Ter
ENST00000685264.1:c.3404G>A (ATP7A)	ENSP00000510136.1:p.Trp1135Ter
ENST00000686033.1:c.3209G>A (ATP7A)	ENSP00000510693.1:p.Trp1070Ter
ENST00000686133.1:c.3404G>A (ATP7A)	ENSP00000509233.1:p.Trp1135Ter
ENST00000686255.1:n.2435G>A (ATP7A)
ENST00000686543.1:c.3170G>A (ATP7A)	ENSP00000509477.1:p.Trp1057Ter
ENST00000687086.1:c.3404G>A (ATP7A)	ENSP00000509566.1:p.Trp1135Ter
ENST00000689514.1:n.1446G>A (ATP7A)
ENST00000689767.1:c.3497G>A (ATP7A)	ENSP00000509406.1:p.Trp1166Ter
ENST00000692908.1:c.3170G>A (ATP7A)	ENSP00000508627.1:p.Trp1057Ter
ENST00000341514.11:c.3404G>A (ATP7A) MANE Select	ENSP00000345728.6:p.Trp1135Ter
ENST00000644362.1:c.-19-76153G>A (PGK1)	ENSP00000496140.1:n.-19-76153G>A
ENST00000645094.1:c.*3318G>A (ATP7A)	ENSP00000493605.1:n.*3318G>A
ENST00000341514.10:c.3404G>A (ATP7A)	ENSP00000345728.6:p.Trp1135Ter
ENST00000343533.9:c.3170G>A (ATP7A)	ENSP00000343026.5:p.Trp1057Ter
ENST00000350425.5:c.*2577G>A (ATP7A)	ENSP00000343678.5:n.*2577G>A
NM_000052.6:c.3404G>A (ATP7A)	NP_000043.4:p.Trp1135Ter
NM_001282224.1:c.3170G>A (ATP7A)	NP_001269153.1:p.Trp1057Ter
NR_104109.1:n.614G>A (ATP7A)
NM_000052.7:c.3404G>A (ATP7A) MANE Select	NP_000043.4:p.Trp1135Ter
NR_104109.2:n.577G>A (ATP7A)
NM_001282224.2:c.3170G>A (ATP7A)	NP_001269153.1:p.Trp1057Ter