Canonical Allele Identifier: CA2439103645

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.78020976G= , CM000685.2:g.78020976G= GRCh38
NC_000023.10:g.77276473G= , CM000685.1:g.77276473G= GRCh37
NC_000023.9:g.77163129G= NCBI36
NG_013224.2:g.115280G=

Transcript Alleles

HGVS Amino-acid change
ENST00000343533.10:c.2843G= (ATP7A) ENSP00000343026.6:p.Ser948=
ENST00000682475.1:n.1230G= (ATP7A)
ENST00000685033.1:c.375+578G= (ATP7A) ENSP00000509269.1:n.375+578G=
ENST00000685264.1:c.2813G= (ATP7A) ENSP00000510136.1:p.Ser938=
ENST00000686033.1:c.2813G= (ATP7A) ENSP00000510693.1:p.Ser938=
ENST00000686133.1:c.2813G= (ATP7A) ENSP00000509233.1:p.Ser938=
ENST00000686255.1:n.1844G= (ATP7A)
ENST00000686543.1:c.2579G= (ATP7A) ENSP00000509477.1:p.Ser860=
ENST00000687086.1:c.2813G= (ATP7A) ENSP00000509566.1:p.Ser938=
ENST00000689514.1:n.855G= (ATP7A)
ENST00000689530.1:c.2813G= (ATP7A) ENSP00000509707.1:p.Ser938=
ENST00000689767.1:c.2906G= (ATP7A) ENSP00000509406.1:p.Ser969=
ENST00000692908.1:c.2579G= (ATP7A) ENSP00000508627.1:p.Ser860=
ENST00000341514.11:c.2813G= (ATP7A) MANE Select ENSP00000345728.6:p.Ser938=
ENST00000644362.1:c.-19-88891G= (PGK1) ENSP00000496140.1:n.-19-88891G=
ENST00000645094.1:c.*2727G= (ATP7A) ENSP00000493605.1:n.*2727G=
ENST00000341514.10:c.2813G= (ATP7A) ENSP00000345728.6:p.Ser938=
ENST00000343533.9:c.2579G= (ATP7A) ENSP00000343026.5:p.Ser860=
ENST00000350425.5:c.*1986G= (ATP7A) ENSP00000343678.5:n.*1986G=
NM_000052.6:c.2813G= (ATP7A) NP_000043.4:p.Ser938=
NM_001282224.1:c.2579G= (ATP7A) NP_001269153.1:p.Ser860=
NR_104109.1:n.322-10424G= (ATP7A)
NM_000052.7:c.2813G= (ATP7A) MANE Select NP_000043.4:p.Ser938=
NR_104109.2:n.285-10424G= (ATP7A)
NM_001282224.2:c.2579G= (ATP7A) NP_001269153.1:p.Ser860=