Canonical Allele Identifier: CA16621511

Linked Data

ClinVar Variation Id: 423830
dbSNP Id: rs1064796648

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.78031425C>T , CM000685.2:g.78031425C>T GRCh38
NC_000023.10:g.77286923C>T , CM000685.1:g.77286923C>T GRCh37
NC_000023.9:g.77173579C>T NCBI36
NG_013224.2:g.125729C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000343533.10:c.3167C>T (ATP7A) ENSP00000343026.6:p.Thr1056Ile
ENST00000682475.1:n.1554C>T (ATP7A)
ENST00000685033.1:c.401C>T (ATP7A) ENSP00000509269.1:p.Thr134Ile
ENST00000685264.1:c.3137C>T (ATP7A) ENSP00000510136.1:p.Thr1046Ile
ENST00000686033.1:c.2942C>T (ATP7A) ENSP00000510693.1:p.Thr981Ile
ENST00000686133.1:c.3137C>T (ATP7A) ENSP00000509233.1:p.Thr1046Ile
ENST00000686255.1:n.2168C>T (ATP7A)
ENST00000686543.1:c.2903C>T (ATP7A) ENSP00000509477.1:p.Thr968Ile
ENST00000687086.1:c.3137C>T (ATP7A) ENSP00000509566.1:p.Thr1046Ile
ENST00000689514.1:n.1179C>T (ATP7A)
ENST00000689767.1:c.3230C>T (ATP7A) ENSP00000509406.1:p.Thr1077Ile
ENST00000692908.1:c.2903C>T (ATP7A) ENSP00000508627.1:p.Thr968Ile
ENST00000341514.11:c.3137C>T (ATP7A) MANE Select ENSP00000345728.6:p.Thr1046Ile
ENST00000644362.1:c.-19-78442C>T (PGK1) ENSP00000496140.1:n.-19-78442C>T
ENST00000645094.1:c.*3051C>T (ATP7A) ENSP00000493605.1:n.*3051C>T
ENST00000341514.10:c.3137C>T (ATP7A) ENSP00000345728.6:p.Thr1046Ile
ENST00000343533.9:c.2903C>T (ATP7A) ENSP00000343026.5:p.Thr968Ile
ENST00000350425.5:c.*2310C>T (ATP7A) ENSP00000343678.5:n.*2310C>T
NM_000052.6:c.3137C>T (ATP7A) NP_000043.4:p.Thr1046Ile
NM_001282224.1:c.2903C>T (ATP7A) NP_001269153.1:p.Thr968Ile
NR_104109.1:n.347C>T (ATP7A)
NM_000052.7:c.3137C>T (ATP7A) MANE Select NP_000043.4:p.Thr1046Ile
NR_104109.2:n.310C>T (ATP7A)
NM_001282224.2:c.2903C>T (ATP7A) NP_001269153.1:p.Thr968Ile