Canonical Allele Identifier: CA2439107640

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.78033722G= , CM000685.2:g.78033722G= GRCh38
NC_000023.10:g.77289220G= , CM000685.1:g.77289220G= GRCh37
NC_000023.9:g.77175876G= NCBI36
NG_013224.2:g.128026G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000343533.10:c.3442G= (ATP7A) ENSP00000343026.6:p.Glu1148=
ENST00000682475.1:n.1829G= (ATP7A)
ENST00000685033.1:c.676G= (ATP7A) ENSP00000509269.1:p.Glu226=
ENST00000685264.1:c.3412G= (ATP7A) ENSP00000510136.1:p.Glu1138=
ENST00000686033.1:c.3217G= (ATP7A) ENSP00000510693.1:p.Glu1073=
ENST00000686133.1:c.3412G= (ATP7A) ENSP00000509233.1:p.Glu1138=
ENST00000686255.1:n.2443G= (ATP7A)
ENST00000686543.1:c.3178G= (ATP7A) ENSP00000509477.1:p.Glu1060=
ENST00000687086.1:c.3412G= (ATP7A) ENSP00000509566.1:p.Glu1138=
ENST00000689514.1:n.1454G= (ATP7A)
ENST00000689767.1:c.3505G= (ATP7A) ENSP00000509406.1:p.Glu1169=
ENST00000692908.1:c.3178G= (ATP7A) ENSP00000508627.1:p.Glu1060=
ENST00000341514.11:c.3412G= (ATP7A) MANE Select ENSP00000345728.6:p.Glu1138=
ENST00000644362.1:c.-19-76145G= (PGK1) ENSP00000496140.1:n.-19-76145G=
ENST00000645094.1:c.*3326G= (ATP7A) ENSP00000493605.1:n.*3326G=
ENST00000341514.10:c.3412G= (ATP7A) ENSP00000345728.6:p.Glu1138=
ENST00000343533.9:c.3178G= (ATP7A) ENSP00000343026.5:p.Glu1060=
ENST00000350425.5:c.*2585G= (ATP7A) ENSP00000343678.5:n.*2585G=
NM_000052.6:c.3412G= (ATP7A) NP_000043.4:p.Glu1138=
NM_001282224.1:c.3178G= (ATP7A) NP_001269153.1:p.Glu1060=
NR_104109.1:n.622G= (ATP7A)
NM_000052.7:c.3412G= (ATP7A) MANE Select NP_000043.4:p.Glu1138=
NR_104109.2:n.585G= (ATP7A)
NM_001282224.2:c.3178G= (ATP7A) NP_001269153.1:p.Glu1060=