Canonical Allele Identifier: CA413603815
Community Standard Title: NM_000052.7(ATP7A):c.3289A>T (p.Lys1097Ter)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.78031577A>T , CM000685.2:g.78031577A>T GRCh38
NC_000023.10:g.77287075A>T , CM000685.1:g.77287075A>T GRCh37
NC_000023.9:g.77173731A>T NCBI36
NG_013224.2:g.125881A>T

Transcript Alleles

HGVS Amino-acid Change
NM_000052.7:c.3289A>T (ATP7A) MANE Select NP_000043.4:p.Lys1097Ter
ENST00000341514.11:c.3289A>T (ATP7A) MANE Select ENSP00000345728.6:p.Lys1097Ter
NM_000052.6:c.3289A>T (ATP7A) NP_000043.4:p.Lys1097Ter
NM_001282224.1:c.3055A>T (ATP7A) NP_001269153.1:p.Lys1019Ter
NM_001282224.2:c.3055A>T (ATP7A) NP_001269153.1:p.Lys1019Ter
NR_104109.1:n.499A>T (ATP7A)
NR_104109.2:n.462A>T (ATP7A)
ENST00000341514.10:c.3289A>T (ATP7A) ENSP00000345728.6:p.Lys1097Ter
ENST00000343533.10:c.3319A>T (ATP7A) ENSP00000343026.6:p.Lys1107Ter
ENST00000343533.9:c.3055A>T (ATP7A) ENSP00000343026.5:p.Lys1019Ter
ENST00000350425.5:c.*2462A>T (ATP7A) ENSP00000343678.5:n.*2462A>T
ENST00000644362.1:c.-19-78290A>T (PGK1) ENSP00000496140.1:n.-19-78290A>T
ENST00000645094.1:c.*3203A>T (ATP7A) ENSP00000493605.1:n.*3203A>T
ENST00000682475.1:n.1706A>T (ATP7A)
ENST00000685033.1:c.553A>T (ATP7A) ENSP00000509269.1:p.Lys185Ter
ENST00000685264.1:c.3289A>T (ATP7A) ENSP00000510136.1:p.Lys1097Ter
ENST00000686033.1:c.3094A>T (ATP7A) ENSP00000510693.1:p.Lys1032Ter
ENST00000686133.1:c.3289A>T (ATP7A) ENSP00000509233.1:p.Lys1097Ter
ENST00000686255.1:n.2320A>T (ATP7A)
ENST00000686543.1:c.3055A>T (ATP7A) ENSP00000509477.1:p.Lys1019Ter
ENST00000687086.1:c.3289A>T (ATP7A) ENSP00000509566.1:p.Lys1097Ter
ENST00000689514.1:n.1331A>T (ATP7A)
ENST00000689767.1:c.3382A>T (ATP7A) ENSP00000509406.1:p.Lys1128Ter
ENST00000692908.1:c.3055A>T (ATP7A) ENSP00000508627.1:p.Lys1019Ter