Canonical Allele Identifier: CA413604064

Gene: ATP7A PGK1

Linked Data

• MyVariant Identifiers: chrX:g.77289205A>G (hg19) ; chrX:g.78033707A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.78033707A>G , CM000685.2:g.78033707A>G	GRCh38
NC_000023.10:g.77289205A>G , CM000685.1:g.77289205A>G	GRCh37
NC_000023.9:g.77175861A>G	NCBI36
NG_013224.2:g.128011A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343533.10:c.3427A>G (ATP7A)	ENSP00000343026.6:p.Asn1143Asp
ENST00000682475.1:n.1814A>G (ATP7A)
ENST00000685033.1:c.661A>G (ATP7A)	ENSP00000509269.1:p.Asn221Asp
ENST00000685264.1:c.3397A>G (ATP7A)	ENSP00000510136.1:p.Asn1133Asp
ENST00000686033.1:c.3202A>G (ATP7A)	ENSP00000510693.1:p.Asn1068Asp
ENST00000686133.1:c.3397A>G (ATP7A)	ENSP00000509233.1:p.Asn1133Asp
ENST00000686255.1:n.2428A>G (ATP7A)
ENST00000686543.1:c.3163A>G (ATP7A)	ENSP00000509477.1:p.Asn1055Asp
ENST00000687086.1:c.3397A>G (ATP7A)	ENSP00000509566.1:p.Asn1133Asp
ENST00000689514.1:n.1439A>G (ATP7A)
ENST00000689767.1:c.3490A>G (ATP7A)	ENSP00000509406.1:p.Asn1164Asp
ENST00000692908.1:c.3163A>G (ATP7A)	ENSP00000508627.1:p.Asn1055Asp
ENST00000341514.11:c.3397A>G (ATP7A) MANE Select	ENSP00000345728.6:p.Asn1133Asp
ENST00000644362.1:c.-19-76160A>G (PGK1)	ENSP00000496140.1:n.-19-76160A>G
ENST00000645094.1:c.*3311A>G (ATP7A)	ENSP00000493605.1:n.*3311A>G
ENST00000341514.10:c.3397A>G (ATP7A)	ENSP00000345728.6:p.Asn1133Asp
ENST00000343533.9:c.3163A>G (ATP7A)	ENSP00000343026.5:p.Asn1055Asp
ENST00000350425.5:c.*2570A>G (ATP7A)	ENSP00000343678.5:n.*2570A>G
NM_000052.6:c.3397A>G (ATP7A)	NP_000043.4:p.Asn1133Asp
NM_001282224.1:c.3163A>G (ATP7A)	NP_001269153.1:p.Asn1055Asp
NR_104109.1:n.607A>G (ATP7A)
NM_000052.7:c.3397A>G (ATP7A) MANE Select	NP_000043.4:p.Asn1133Asp
NR_104109.2:n.570A>G (ATP7A)
NM_001282224.2:c.3163A>G (ATP7A)	NP_001269153.1:p.Asn1055Asp