Canonical Allele Identifier: CA413598391

Gene: ATP7A PGK1

Linked Data

• COSMIC: COSM5878340 ; COSM5878341
• MyVariant Identifiers: chrX:g.77267085C>T (hg19) ; chrX:g.78011588C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.78011588C>T , CM000685.2:g.78011588C>T	GRCh38
NC_000023.10:g.77267085C>T , CM000685.1:g.77267085C>T	GRCh37
NC_000023.9:g.77153741C>T	NCBI36
NG_013224.2:g.105892C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000343533.10:c.2116C>T (ATP7A)	ENSP00000343026.6:p.His706Tyr
ENST00000682475.1:n.737C>T (ATP7A)
ENST00000685264.1:c.2086C>T (ATP7A)	ENSP00000510136.1:p.His696Tyr
ENST00000686033.1:c.2086C>T (ATP7A)	ENSP00000510693.1:p.His696Tyr
ENST00000686133.1:c.2086C>T (ATP7A)	ENSP00000509233.1:p.His696Tyr
ENST00000686255.1:n.1117C>T (ATP7A)
ENST00000686480.1:c.2086C>T (ATP7A)	ENSP00000508978.1:p.His696Tyr
ENST00000686515.1:n.2226C>T (ATP7A)
ENST00000686543.1:c.2086C>T (ATP7A)	ENSP00000509477.1:p.His696Tyr
ENST00000686688.1:c.2086C>T (ATP7A)	ENSP00000509416.1:p.His696Tyr
ENST00000686999.1:n.2397C>T (ATP7A)
ENST00000687086.1:c.2086C>T (ATP7A)	ENSP00000509566.1:p.His696Tyr
ENST00000687628.1:n.4295C>T (ATP7A)
ENST00000688746.1:n.2238C>T (ATP7A)
ENST00000689514.1:n.128C>T (ATP7A)
ENST00000689530.1:c.2086C>T (ATP7A)	ENSP00000509707.1:p.His696Tyr
ENST00000689649.1:c.2086C>T (ATP7A)	ENSP00000509277.1:p.His696Tyr
ENST00000689767.1:c.2179C>T (ATP7A)	ENSP00000509406.1:p.His727Tyr
ENST00000689872.1:c.*35C>T (ATP7A)	ENSP00000509373.1:n.*35C>T
ENST00000692110.1:c.2002C>T (ATP7A)	ENSP00000509366.1:p.His668Tyr
ENST00000692908.1:c.2086C>T (ATP7A)	ENSP00000508627.1:p.His696Tyr
ENST00000693398.1:c.2086C>T (ATP7A)	ENSP00000510089.1:p.His696Tyr
ENST00000341514.11:c.2086C>T (ATP7A) MANE Select	ENSP00000345728.6:p.His696Tyr
ENST00000644362.1:c.-19-98279C>T (PGK1)	ENSP00000496140.1:n.-19-98279C>T
ENST00000645094.1:c.*2000C>T (ATP7A)	ENSP00000493605.1:n.*2000C>T
ENST00000341514.10:c.2086C>T (ATP7A)	ENSP00000345728.6:p.His696Tyr
ENST00000343533.9:c.2086C>T (ATP7A)	ENSP00000343026.5:p.His696Tyr
ENST00000350425.5:c.*1259C>T (ATP7A)	ENSP00000343678.5:n.*1259C>T
NM_000052.6:c.2086C>T (ATP7A)	NP_000043.4:p.His696Tyr
NM_001282224.1:c.2086C>T (ATP7A)	NP_001269153.1:p.His696Tyr
NR_104109.1:n.322-19812C>T (ATP7A)
NM_000052.7:c.2086C>T (ATP7A) MANE Select	NP_000043.4:p.His696Tyr
NR_104109.2:n.285-19812C>T (ATP7A)
NM_001282224.2:c.2086C>T (ATP7A)	NP_001269153.1:p.His696Tyr