Canonical Allele Identifier: CA413604124

Gene: ATP7A PGK1

Linked Data

• MyVariant Identifiers: chrX:g.77289228T>G (hg19) ; chrX:g.78033730T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.78033730T>G , CM000685.2:g.78033730T>G	GRCh38
NC_000023.10:g.77289228T>G , CM000685.1:g.77289228T>G	GRCh37
NC_000023.9:g.77175884T>G	NCBI36
NG_013224.2:g.128034T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343533.10:c.3450T>G (ATP7A)	ENSP00000343026.6:p.Asn1150Lys
ENST00000682475.1:n.1837T>G (ATP7A)
ENST00000685033.1:c.684T>G (ATP7A)	ENSP00000509269.1:p.Asn228Lys
ENST00000685264.1:c.3420T>G (ATP7A)	ENSP00000510136.1:p.Asn1140Lys
ENST00000686033.1:c.3225T>G (ATP7A)	ENSP00000510693.1:p.Asn1075Lys
ENST00000686133.1:c.3420T>G (ATP7A)	ENSP00000509233.1:p.Asn1140Lys
ENST00000686255.1:n.2451T>G (ATP7A)
ENST00000686543.1:c.3186T>G (ATP7A)	ENSP00000509477.1:p.Asn1062Lys
ENST00000687086.1:c.3420T>G (ATP7A)	ENSP00000509566.1:p.Asn1140Lys
ENST00000689514.1:n.1462T>G (ATP7A)
ENST00000689767.1:c.3513T>G (ATP7A)	ENSP00000509406.1:p.Asn1171Lys
ENST00000692908.1:c.3186T>G (ATP7A)	ENSP00000508627.1:p.Asn1062Lys
ENST00000341514.11:c.3420T>G (ATP7A) MANE Select	ENSP00000345728.6:p.Asn1140Lys
ENST00000644362.1:c.-19-76137T>G (PGK1)	ENSP00000496140.1:n.-19-76137T>G
ENST00000645094.1:c.*3334T>G (ATP7A)	ENSP00000493605.1:n.*3334T>G
ENST00000341514.10:c.3420T>G (ATP7A)	ENSP00000345728.6:p.Asn1140Lys
ENST00000343533.9:c.3186T>G (ATP7A)	ENSP00000343026.5:p.Asn1062Lys
ENST00000350425.5:c.*2593T>G (ATP7A)	ENSP00000343678.5:n.*2593T>G
NM_000052.6:c.3420T>G (ATP7A)	NP_000043.4:p.Asn1140Lys
NM_001282224.1:c.3186T>G (ATP7A)	NP_001269153.1:p.Asn1062Lys
NR_104109.1:n.630T>G (ATP7A)
NM_000052.7:c.3420T>G (ATP7A) MANE Select	NP_000043.4:p.Asn1140Lys
NR_104109.2:n.593T>G (ATP7A)
NM_001282224.2:c.3186T>G (ATP7A)	NP_001269153.1:p.Asn1062Lys