Canonical Allele Identifier: CA10459531
Community Standard Title: NM_000052.7(ATP7A):c.4246G>A (p.Glu1416Lys)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.78046313G>A , CM000685.2:g.78046313G>A GRCh38
NC_000023.10:g.77301810G>A , CM000685.1:g.77301810G>A GRCh37
NC_000023.9:g.77188466G>A NCBI36
NG_013224.2:g.140617G>A

Transcript Alleles

HGVS Amino-acid Change
NM_000052.7:c.4246G>A (ATP7A) MANE Select NP_000043.4:p.Glu1416Lys
ENST00000341514.11:c.4246G>A (ATP7A) MANE Select ENSP00000345728.6:p.Glu1416Lys
NM_000052.6:c.4246G>A (ATP7A) NP_000043.4:p.Glu1416Lys
NM_001282224.1:c.4012G>A (ATP7A) NP_001269153.1:p.Glu1338Lys
NM_001282224.2:c.4012G>A (ATP7A) NP_001269153.1:p.Glu1338Lys
NR_104109.1:n.1456G>A (ATP7A)
NR_104109.2:n.1419G>A (ATP7A)
ENST00000341514.10:c.4246G>A (ATP7A) ENSP00000345728.6:p.Glu1416Lys
ENST00000343533.10:c.4276G>A (ATP7A) ENSP00000343026.6:p.Glu1426Lys
ENST00000343533.9:c.4012G>A (ATP7A) ENSP00000343026.5:p.Glu1338Lys
ENST00000350425.5:c.*3419G>A (ATP7A) ENSP00000343678.5:n.*3419G>A
ENST00000644362.1:c.-19-63554G>A (PGK1) ENSP00000496140.1:n.-19-63554G>A
ENST00000682475.1:n.2663G>A (ATP7A)
ENST00000685033.1:c.1510G>A (ATP7A) ENSP00000509269.1:p.Glu504Lys
ENST00000685264.1:c.4246G>A (ATP7A) ENSP00000510136.1:p.Glu1416Lys
ENST00000686033.1:c.4051G>A (ATP7A) ENSP00000510693.1:p.Glu1351Lys
ENST00000686133.1:c.4246G>A (ATP7A) ENSP00000509233.1:p.Glu1416Lys
ENST00000686255.1:n.3277G>A (ATP7A)
ENST00000686543.1:c.4012G>A (ATP7A) ENSP00000509477.1:p.Glu1338Lys
ENST00000687086.1:c.4246G>A (ATP7A) ENSP00000509566.1:p.Glu1416Lys
ENST00000689083.1:n.1541G>A (ATP7A)
ENST00000689767.1:c.4339G>A (ATP7A) ENSP00000509406.1:p.Glu1447Lys
ENST00000692908.1:c.4012G>A (ATP7A) ENSP00000508627.1:p.Glu1338Lys