Canonical Allele Identifier: CA2439103606

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.78020888C= , CM000685.2:g.78020888C= GRCh38
NC_000023.10:g.77276385C= , CM000685.1:g.77276385C= GRCh37
NC_000023.9:g.77163041C= NCBI36
NG_013224.2:g.115192C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000343533.10:c.2812-57C= (ATP7A) ENSP00000343026.6:n.2812-57C=
ENST00000682475.1:n.1199-57C= (ATP7A)
ENST00000685033.1:c.375+490C= (ATP7A) ENSP00000509269.1:n.375+490C=
ENST00000685264.1:c.2782-57C= (ATP7A) ENSP00000510136.1:n.2782-57C=
ENST00000686033.1:c.2782-57C= (ATP7A) ENSP00000510693.1:n.2782-57C=
ENST00000686133.1:c.2782-57C= (ATP7A) ENSP00000509233.1:n.2782-57C=
ENST00000686255.1:n.1813-57C= (ATP7A)
ENST00000686543.1:c.2548-57C= (ATP7A) ENSP00000509477.1:n.2548-57C=
ENST00000687086.1:c.2782-57C= (ATP7A) ENSP00000509566.1:n.2782-57C=
ENST00000689514.1:n.824-57C= (ATP7A)
ENST00000689530.1:c.2782-57C= (ATP7A) ENSP00000509707.1:n.2782-57C=
ENST00000689767.1:c.2875-57C= (ATP7A) ENSP00000509406.1:n.2875-57C=
ENST00000692908.1:c.2548-57C= (ATP7A) ENSP00000508627.1:n.2548-57C=
ENST00000341514.11:c.2782-57C= (ATP7A) MANE Select ENSP00000345728.6:n.2782-57C=
ENST00000644362.1:c.-19-88979C= (PGK1) ENSP00000496140.1:n.-19-88979C=
ENST00000645094.1:c.*2696-57C= (ATP7A) ENSP00000493605.1:n.*2696-57C=
ENST00000341514.10:c.2782-57C= (ATP7A) ENSP00000345728.6:n.2782-57C=
ENST00000343533.9:c.2548-57C= (ATP7A) ENSP00000343026.5:n.2548-57C=
ENST00000350425.5:c.*1955-57C= (ATP7A) ENSP00000343678.5:n.*1955-57C=
NM_000052.6:c.2782-57C= (ATP7A) NP_000043.4:n.2782-57C=
NM_001282224.1:c.2548-57C= (ATP7A) NP_001269153.1:n.2548-57C=
NR_104109.1:n.322-10512C= (ATP7A)
NM_000052.7:c.2782-57C= (ATP7A) MANE Select NP_000043.4:n.2782-57C=
NR_104109.2:n.285-10512C= (ATP7A)
NM_001282224.2:c.2548-57C= (ATP7A) NP_001269153.1:n.2548-57C=