Canonical Allele Identifier: CA413597917

Gene: ATP7A PGK1

Linked Data

• MyVariant Identifiers: chrX:g.77266683T>C (hg19) ; chrX:g.78011186T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.78011186T>C , CM000685.2:g.78011186T>C	GRCh38
NC_000023.10:g.77266683T>C , CM000685.1:g.77266683T>C	GRCh37
NC_000023.9:g.77153339T>C	NCBI36
NG_013224.2:g.105490T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000343533.10:c.1910T>C (ATP7A)	ENSP00000343026.6:p.Phe637Ser
ENST00000682475.1:n.335T>C (ATP7A)
ENST00000685264.1:c.1880T>C (ATP7A)	ENSP00000510136.1:p.Phe627Ser
ENST00000686033.1:c.1880T>C (ATP7A)	ENSP00000510693.1:p.Phe627Ser
ENST00000686133.1:c.1880T>C (ATP7A)	ENSP00000509233.1:p.Phe627Ser
ENST00000686255.1:n.715T>C (ATP7A)
ENST00000686480.1:c.1880T>C (ATP7A)	ENSP00000508978.1:p.Phe627Ser
ENST00000686515.1:n.2020T>C (ATP7A)
ENST00000686543.1:c.1880T>C (ATP7A)	ENSP00000509477.1:p.Phe627Ser
ENST00000686688.1:c.1880T>C (ATP7A)	ENSP00000509416.1:p.Phe627Ser
ENST00000686999.1:n.2191T>C (ATP7A)
ENST00000687086.1:c.1880T>C (ATP7A)	ENSP00000509566.1:p.Phe627Ser
ENST00000687628.1:n.3893T>C (ATP7A)
ENST00000688746.1:n.2032T>C (ATP7A)
ENST00000689530.1:c.1880T>C (ATP7A)	ENSP00000509707.1:p.Phe627Ser
ENST00000689649.1:c.1880T>C (ATP7A)	ENSP00000509277.1:p.Phe627Ser
ENST00000689767.1:c.1973T>C (ATP7A)	ENSP00000509406.1:p.Phe658Ser
ENST00000689872.1:c.1870-263T>C (ATP7A)	ENSP00000509373.1:n.1870-263T>C
ENST00000692110.1:c.1796T>C (ATP7A)	ENSP00000509366.1:p.Phe599Ser
ENST00000692908.1:c.1880T>C (ATP7A)	ENSP00000508627.1:p.Phe627Ser
ENST00000693398.1:c.1880T>C (ATP7A)	ENSP00000510089.1:p.Phe627Ser
ENST00000341514.11:c.1880T>C (ATP7A) MANE Select	ENSP00000345728.6:p.Phe627Ser
ENST00000644362.1:c.-19-98681T>C (PGK1)	ENSP00000496140.1:n.-19-98681T>C
ENST00000645094.1:c.*1794T>C (ATP7A)	ENSP00000493605.1:n.*1794T>C
ENST00000341514.10:c.1880T>C (ATP7A)	ENSP00000345728.6:p.Phe627Ser
ENST00000343533.9:c.1880T>C (ATP7A)	ENSP00000343026.5:p.Phe627Ser
ENST00000350425.5:c.*1053T>C (ATP7A)	ENSP00000343678.5:n.*1053T>C
NM_000052.6:c.1880T>C (ATP7A)	NP_000043.4:p.Phe627Ser
NM_001282224.1:c.1880T>C (ATP7A)	NP_001269153.1:p.Phe627Ser
NR_104109.1:n.322-20214T>C (ATP7A)
NM_000052.7:c.1880T>C (ATP7A) MANE Select	NP_000043.4:p.Phe627Ser
NR_104109.2:n.285-20214T>C (ATP7A)
NM_001282224.2:c.1880T>C (ATP7A)	NP_001269153.1:p.Phe627Ser