Canonical Allele Identifier: CA2840914971

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.78045444C>A , CM000685.2:g.78045444C>A GRCh38
NC_000023.10:g.77300941C>A , CM000685.1:g.77300941C>A GRCh37
NC_000023.9:g.77187597C>A NCBI36
NG_013224.2:g.139748C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000343533.10:c.4154-26C>A (ATP7A) ENSP00000343026.6:n.4154-26C>A
ENST00000682475.1:n.2541-26C>A (ATP7A)
ENST00000685033.1:c.1388-26C>A (ATP7A) ENSP00000509269.1:n.1388-26C>A
ENST00000685264.1:c.4124-26C>A (ATP7A) ENSP00000510136.1:n.4124-26C>A
ENST00000686033.1:c.3929-26C>A (ATP7A) ENSP00000510693.1:n.3929-26C>A
ENST00000686133.1:c.4124-26C>A (ATP7A) ENSP00000509233.1:n.4124-26C>A
ENST00000686255.1:n.3155-26C>A (ATP7A)
ENST00000686543.1:c.3890-26C>A (ATP7A) ENSP00000509477.1:n.3890-26C>A
ENST00000687086.1:c.4124-26C>A (ATP7A) ENSP00000509566.1:n.4124-26C>A
ENST00000689083.1:n.1393C>A (ATP7A)
ENST00000689767.1:c.4217-26C>A (ATP7A) ENSP00000509406.1:n.4217-26C>A
ENST00000692908.1:c.3890-26C>A (ATP7A) ENSP00000508627.1:n.3890-26C>A
ENST00000341514.11:c.4124-26C>A (ATP7A) MANE Select ENSP00000345728.6:n.4124-26C>A
ENST00000644362.1:c.-19-64423C>A (PGK1) ENSP00000496140.1:n.-19-64423C>A
ENST00000341514.10:c.4124-26C>A (ATP7A) ENSP00000345728.6:n.4124-26C>A
ENST00000343533.9:c.3890-26C>A (ATP7A) ENSP00000343026.5:n.3890-26C>A
ENST00000350425.5:c.*3297-26C>A (ATP7A) ENSP00000343678.5:n.*3297-26C>A
NM_000052.6:c.4124-26C>A (ATP7A) NP_000043.4:n.4124-26C>A
NM_001282224.1:c.3890-26C>A (ATP7A) NP_001269153.1:n.3890-26C>A
NR_104109.1:n.1334-26C>A (ATP7A)
NM_000052.7:c.4124-26C>A (ATP7A) MANE Select NP_000043.4:n.4124-26C>A
NR_104109.2:n.1297-26C>A (ATP7A)
NM_001282224.2:c.3890-26C>A (ATP7A) NP_001269153.1:n.3890-26C>A