Canonical Allele Identifier: CA413604445
Community Standard Title: NM_000052.7(ATP7A):c.3560G>A (p.Trp1187Ter)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.78038884G>A , CM000685.2:g.78038884G>A GRCh38
NC_000023.10:g.77294382G>A , CM000685.1:g.77294382G>A GRCh37
NC_000023.9:g.77181038G>A NCBI36
NG_013224.2:g.133188G>A

Transcript Alleles

HGVS Amino-acid Change
NM_000052.7:c.3560G>A (ATP7A) MANE Select NP_000043.4:p.Trp1187Ter
ENST00000341514.11:c.3560G>A (ATP7A) MANE Select ENSP00000345728.6:p.Trp1187Ter
NM_000052.6:c.3560G>A (ATP7A) NP_000043.4:p.Trp1187Ter
NM_001282224.1:c.3326G>A (ATP7A) NP_001269153.1:p.Trp1109Ter
NM_001282224.2:c.3326G>A (ATP7A) NP_001269153.1:p.Trp1109Ter
NR_104109.1:n.770G>A (ATP7A)
NR_104109.2:n.733G>A (ATP7A)
ENST00000341514.10:c.3560G>A (ATP7A) ENSP00000345728.6:p.Trp1187Ter
ENST00000343533.10:c.3590G>A (ATP7A) ENSP00000343026.6:p.Trp1197Ter
ENST00000343533.9:c.3326G>A (ATP7A) ENSP00000343026.5:p.Trp1109Ter
ENST00000350425.5:c.*2733G>A (ATP7A) ENSP00000343678.5:n.*2733G>A
ENST00000644362.1:c.-19-70983G>A (PGK1) ENSP00000496140.1:n.-19-70983G>A
ENST00000645094.1:c.*3474G>A (ATP7A) ENSP00000493605.1:n.*3474G>A
ENST00000682475.1:n.1977G>A (ATP7A)
ENST00000685033.1:c.824G>A (ATP7A) ENSP00000509269.1:p.Trp275Ter
ENST00000685264.1:c.3560G>A (ATP7A) ENSP00000510136.1:p.Trp1187Ter
ENST00000686033.1:c.3365G>A (ATP7A) ENSP00000510693.1:p.Trp1122Ter
ENST00000686133.1:c.3560G>A (ATP7A) ENSP00000509233.1:p.Trp1187Ter
ENST00000686255.1:n.2591G>A (ATP7A)
ENST00000686543.1:c.3326G>A (ATP7A) ENSP00000509477.1:p.Trp1109Ter
ENST00000687086.1:c.3560G>A (ATP7A) ENSP00000509566.1:p.Trp1187Ter
ENST00000689514.1:n.1602G>A (ATP7A)
ENST00000689767.1:c.3653G>A (ATP7A) ENSP00000509406.1:p.Trp1218Ter
ENST00000692908.1:c.3326G>A (ATP7A) ENSP00000508627.1:p.Trp1109Ter