Canonical Allele Identifier: CA277311

Linked Data

ClinVar Variation Id: 210386
ClinVar RCV Id: RCV000194386
dbSNP Id: rs797045325

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.77989628G>T , CM000685.2:g.77989628G>T GRCh38
NC_000023.10:g.77245124G>T , CM000685.1:g.77245124G>T GRCh37
NC_000023.9:g.77131780G>T NCBI36
NG_013224.2:g.83932G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000343533.10:c.1036G>T (ATP7A) ENSP00000343026.6:p.Glu346Ter
ENST00000682742.2:n.1168G>T (ATP7A)
ENST00000685208.1:n.1669G>T (ATP7A)
ENST00000685264.1:c.1006G>T (ATP7A) ENSP00000510136.1:p.Glu336Ter
ENST00000685434.1:n.1124G>T (ATP7A)
ENST00000685885.1:c.1042G>T (ATP7A) ENSP00000510005.1:p.Glu348Ter
ENST00000686033.1:c.1006G>T (ATP7A) ENSP00000510693.1:p.Glu336Ter
ENST00000686133.1:c.1006G>T (ATP7A) ENSP00000509233.1:p.Glu336Ter
ENST00000686416.1:n.1360G>T (ATP7A)
ENST00000686480.1:c.1006G>T (ATP7A) ENSP00000508978.1:p.Glu336Ter
ENST00000686515.1:n.1146G>T (ATP7A)
ENST00000686543.1:c.1006G>T (ATP7A) ENSP00000509477.1:p.Glu336Ter
ENST00000686688.1:c.1006G>T (ATP7A) ENSP00000509416.1:p.Glu336Ter
ENST00000686999.1:n.1317G>T (ATP7A)
ENST00000687086.1:c.1006G>T (ATP7A) ENSP00000509566.1:p.Glu336Ter
ENST00000687416.1:c.1006G>T (ATP7A) ENSP00000510310.1:p.Glu336Ter
ENST00000687599.1:c.1006G>T (ATP7A) ENSP00000508745.1:p.Glu336Ter
ENST00000687628.1:n.1107G>T (ATP7A)
ENST00000687984.1:c.1006G>T (ATP7A) ENSP00000510772.1:p.Glu336Ter
ENST00000688249.1:c.1006G>T (ATP7A) ENSP00000510644.1:p.Glu336Ter
ENST00000688338.1:c.1006G>T (ATP7A) ENSP00000508672.1:p.Glu336Ter
ENST00000688746.1:n.1158G>T (ATP7A)
ENST00000688889.1:c.*920G>T (ATP7A) ENSP00000508610.1:n.*920G>T
ENST00000689530.1:c.1006G>T (ATP7A) ENSP00000509707.1:p.Glu336Ter
ENST00000689541.1:n.1315G>T (ATP7A)
ENST00000689649.1:c.1006G>T (ATP7A) ENSP00000509277.1:p.Glu336Ter
ENST00000689767.1:c.1006G>T (ATP7A) ENSP00000509406.1:p.Glu336Ter
ENST00000689872.1:c.1006G>T (ATP7A) ENSP00000509373.1:p.Glu336Ter
ENST00000689891.1:c.1006G>T (ATP7A) ENSP00000508974.1:p.Glu336Ter
ENST00000691152.1:c.1006G>T (ATP7A) ENSP00000508843.1:p.Glu336Ter
ENST00000691456.1:n.1297G>T (ATP7A)
ENST00000692110.1:c.1006G>T (ATP7A) ENSP00000509366.1:p.Glu336Ter
ENST00000692908.1:c.1006G>T (ATP7A) ENSP00000508627.1:p.Glu336Ter
ENST00000693051.1:c.1006G>T (ATP7A) ENSP00000510332.1:p.Glu336Ter
ENST00000693387.1:c.*935G>T (ATP7A) ENSP00000508732.1:n.*935G>T
ENST00000693398.1:c.1006G>T (ATP7A) ENSP00000510089.1:p.Glu336Ter
ENST00000341514.11:c.1006G>T (ATP7A) MANE Select ENSP00000345728.6:p.Glu336Ter
ENST00000644362.1:c.-20+78793G>T (PGK1) ENSP00000496140.1:n.-20+78793G>T
ENST00000645094.1:c.*920G>T (ATP7A) ENSP00000493605.1:n.*920G>T
ENST00000341514.10:c.1006G>T (ATP7A) ENSP00000345728.6:p.Glu336Ter
ENST00000343533.9:c.1006G>T (ATP7A) ENSP00000343026.5:p.Glu336Ter
ENST00000350425.5:c.*179G>T (ATP7A) ENSP00000343678.5:n.*179G>T
NM_000052.6:c.1006G>T (ATP7A) NP_000043.4:p.Glu336Ter
NM_001282224.1:c.1006G>T (ATP7A) NP_001269153.1:p.Glu336Ter
NR_104109.1:n.321+17867G>T (ATP7A)
NM_000052.7:c.1006G>T (ATP7A) MANE Select NP_000043.4:p.Glu336Ter
NR_104109.2:n.284+17867G>T (ATP7A)
NM_001282224.2:c.1006G>T (ATP7A) NP_001269153.1:p.Glu336Ter