Canonical Allele Identifier: CA1134515211

Linked Data

dbSNP Id: rs2077995218
gnomAD v3: X-78033547-A-T
gnomAD v4: X-78033547-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.78033547A>T , CM000685.2:g.78033547A>T GRCh38
NC_000023.10:g.77289045A>T , CM000685.1:g.77289045A>T GRCh37
NC_000023.9:g.77175701A>T NCBI36
NG_013224.2:g.127851A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000343533.10:c.3325-58A>T (ATP7A) ENSP00000343026.6:n.3325-58A>T
ENST00000682475.1:n.1712-58A>T (ATP7A)
ENST00000685033.1:c.559-58A>T (ATP7A) ENSP00000509269.1:n.559-58A>T
ENST00000685264.1:c.3295-58A>T (ATP7A) ENSP00000510136.1:n.3295-58A>T
ENST00000686033.1:c.3100-58A>T (ATP7A) ENSP00000510693.1:n.3100-58A>T
ENST00000686133.1:c.3295-58A>T (ATP7A) ENSP00000509233.1:n.3295-58A>T
ENST00000686255.1:n.2326-58A>T (ATP7A)
ENST00000686543.1:c.3061-58A>T (ATP7A) ENSP00000509477.1:n.3061-58A>T
ENST00000687086.1:c.3295-58A>T (ATP7A) ENSP00000509566.1:n.3295-58A>T
ENST00000689514.1:n.1337-58A>T (ATP7A)
ENST00000689767.1:c.3388-58A>T (ATP7A) ENSP00000509406.1:n.3388-58A>T
ENST00000692908.1:c.3061-58A>T (ATP7A) ENSP00000508627.1:n.3061-58A>T
ENST00000341514.11:c.3295-58A>T (ATP7A) MANE Select ENSP00000345728.6:n.3295-58A>T
ENST00000644362.1:c.-19-76320A>T (PGK1) ENSP00000496140.1:n.-19-76320A>T
ENST00000645094.1:c.*3209-58A>T (ATP7A) ENSP00000493605.1:n.*3209-58A>T
ENST00000341514.10:c.3295-58A>T (ATP7A) ENSP00000345728.6:n.3295-58A>T
ENST00000343533.9:c.3061-58A>T (ATP7A) ENSP00000343026.5:n.3061-58A>T
ENST00000350425.5:c.*2468-58A>T (ATP7A) ENSP00000343678.5:n.*2468-58A>T
NM_000052.6:c.3295-58A>T (ATP7A) NP_000043.4:n.3295-58A>T
NM_001282224.1:c.3061-58A>T (ATP7A) NP_001269153.1:n.3061-58A>T
NR_104109.1:n.505-58A>T (ATP7A)
NM_000052.7:c.3295-58A>T (ATP7A) MANE Select NP_000043.4:n.3295-58A>T
NR_104109.2:n.468-58A>T (ATP7A)
NM_001282224.2:c.3061-58A>T (ATP7A) NP_001269153.1:n.3061-58A>T