Canonical Allele Identifier: CA517057395

Gene: ATP7A PGK1

Linked Data

• MyVariant Identifiers: chrX:g.77264706T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.78009209T>C , CM000685.2:g.78009209T>C	GRCh38
NC_000023.10:g.77264706T>C , CM000685.1:g.77264706T>C	GRCh37
NC_000023.9:g.77151362T>C	NCBI36
NG_013224.2:g.103513T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343533.10:c.1845T>C (ATP7A)	ENSP00000343026.6:p.His615=
ENST00000682742.2:n.1977T>C (ATP7A)
ENST00000685264.1:c.1815T>C (ATP7A)	ENSP00000510136.1:p.His605=
ENST00000685434.1:n.1849T>C (ATP7A)
ENST00000686033.1:c.1815T>C (ATP7A)	ENSP00000510693.1:p.His605=
ENST00000686133.1:c.1815T>C (ATP7A)	ENSP00000509233.1:p.His605=
ENST00000686416.1:n.2169T>C (ATP7A)
ENST00000686480.1:c.1815T>C (ATP7A)	ENSP00000508978.1:p.His605=
ENST00000686515.1:n.1955T>C (ATP7A)
ENST00000686543.1:c.1815T>C (ATP7A)	ENSP00000509477.1:p.His605=
ENST00000686688.1:c.1815T>C (ATP7A)	ENSP00000509416.1:p.His605=
ENST00000686999.1:n.2126T>C (ATP7A)
ENST00000687086.1:c.1815T>C (ATP7A)	ENSP00000509566.1:p.His605=
ENST00000687628.1:n.1916T>C (ATP7A)
ENST00000688746.1:n.1967T>C (ATP7A)
ENST00000689530.1:c.1815T>C (ATP7A)	ENSP00000509707.1:p.His605=
ENST00000689541.1:n.2124T>C (ATP7A)
ENST00000689649.1:c.1815T>C (ATP7A)	ENSP00000509277.1:p.His605=
ENST00000689767.1:c.1908T>C (ATP7A)	ENSP00000509406.1:p.His636=
ENST00000689872.1:c.1815T>C (ATP7A)	ENSP00000509373.1:p.His605=
ENST00000692110.1:c.1731T>C (ATP7A)	ENSP00000509366.1:p.His577=
ENST00000692908.1:c.1815T>C (ATP7A)	ENSP00000508627.1:p.His605=
ENST00000693387.1:c.*1744T>C (ATP7A)	ENSP00000508732.1:n.*1744T>C
ENST00000693398.1:c.1815T>C (ATP7A)	ENSP00000510089.1:p.His605=
ENST00000341514.11:c.1815T>C (ATP7A) MANE Select	ENSP00000345728.6:p.His605=
ENST00000644362.1:c.-20+98374T>C (PGK1)	ENSP00000496140.1:n.-20+98374T>C
ENST00000645094.1:c.*1729T>C (ATP7A)	ENSP00000493605.1:n.*1729T>C
ENST00000341514.10:c.1815T>C (ATP7A)	ENSP00000345728.6:p.His605=
ENST00000343533.9:c.1815T>C (ATP7A)	ENSP00000343026.5:p.His605=
ENST00000350425.5:c.*988T>C (ATP7A)	ENSP00000343678.5:n.*988T>C
NM_000052.6:c.1815T>C (ATP7A)	NP_000043.4:p.His605=
NM_001282224.1:c.1815T>C (ATP7A)	NP_001269153.1:p.His605=
NR_104109.1:n.322-22191T>C (ATP7A)
NM_000052.7:c.1815T>C (ATP7A) MANE Select	NP_000043.4:p.His605=
NR_104109.2:n.285-22191T>C (ATP7A)
NM_001282224.2:c.1815T>C (ATP7A)	NP_001269153.1:p.His605=