Canonical Allele Identifier: CA413598145

Gene: ATP7A PGK1

Linked Data

• MyVariant Identifiers: chrX:g.77266981G>C (hg19) ; chrX:g.78011484G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.78011484G>C , CM000685.2:g.78011484G>C	GRCh38
NC_000023.10:g.77266981G>C , CM000685.1:g.77266981G>C	GRCh37
NC_000023.9:g.77153637G>C	NCBI36
NG_013224.2:g.105788G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343533.10:c.2012G>C (ATP7A)	ENSP00000343026.6:p.Cys671Ser
ENST00000682475.1:n.633G>C (ATP7A)
ENST00000685264.1:c.1982G>C (ATP7A)	ENSP00000510136.1:p.Cys661Ser
ENST00000686033.1:c.1982G>C (ATP7A)	ENSP00000510693.1:p.Cys661Ser
ENST00000686133.1:c.1982G>C (ATP7A)	ENSP00000509233.1:p.Cys661Ser
ENST00000686255.1:n.1013G>C (ATP7A)
ENST00000686480.1:c.1982G>C (ATP7A)	ENSP00000508978.1:p.Cys661Ser
ENST00000686515.1:n.2122G>C (ATP7A)
ENST00000686543.1:c.1982G>C (ATP7A)	ENSP00000509477.1:p.Cys661Ser
ENST00000686688.1:c.1982G>C (ATP7A)	ENSP00000509416.1:p.Cys661Ser
ENST00000686999.1:n.2293G>C (ATP7A)
ENST00000687086.1:c.1982G>C (ATP7A)	ENSP00000509566.1:p.Cys661Ser
ENST00000687628.1:n.4191G>C (ATP7A)
ENST00000688746.1:n.2134G>C (ATP7A)
ENST00000689514.1:n.24G>C (ATP7A)
ENST00000689530.1:c.1982G>C (ATP7A)	ENSP00000509707.1:p.Cys661Ser
ENST00000689649.1:c.1982G>C (ATP7A)	ENSP00000509277.1:p.Cys661Ser
ENST00000689767.1:c.2075G>C (ATP7A)	ENSP00000509406.1:p.Cys692Ser
ENST00000689872.1:c.1905G>C (ATP7A)	ENSP00000509373.1:p.Leu635=
ENST00000692110.1:c.1898G>C (ATP7A)	ENSP00000509366.1:p.Cys633Ser
ENST00000692908.1:c.1982G>C (ATP7A)	ENSP00000508627.1:p.Cys661Ser
ENST00000693398.1:c.1982G>C (ATP7A)	ENSP00000510089.1:p.Cys661Ser
ENST00000341514.11:c.1982G>C (ATP7A) MANE Select	ENSP00000345728.6:p.Cys661Ser
ENST00000644362.1:c.-19-98383G>C (PGK1)	ENSP00000496140.1:n.-19-98383G>C
ENST00000645094.1:c.*1896G>C (ATP7A)	ENSP00000493605.1:n.*1896G>C
ENST00000341514.10:c.1982G>C (ATP7A)	ENSP00000345728.6:p.Cys661Ser
ENST00000343533.9:c.1982G>C (ATP7A)	ENSP00000343026.5:p.Cys661Ser
ENST00000350425.5:c.*1155G>C (ATP7A)	ENSP00000343678.5:n.*1155G>C
NM_000052.6:c.1982G>C (ATP7A)	NP_000043.4:p.Cys661Ser
NM_001282224.1:c.1982G>C (ATP7A)	NP_001269153.1:p.Cys661Ser
NR_104109.1:n.322-19916G>C (ATP7A)
NM_000052.7:c.1982G>C (ATP7A) MANE Select	NP_000043.4:p.Cys661Ser
NR_104109.2:n.285-19916G>C (ATP7A)
NM_001282224.2:c.1982G>C (ATP7A)	NP_001269153.1:p.Cys661Ser