Canonical Allele Identifier: CA2439107628

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.78033674A= , CM000685.2:g.78033674A= GRCh38
NC_000023.10:g.77289172A= , CM000685.1:g.77289172A= GRCh37
NC_000023.9:g.77175828A= NCBI36
NG_013224.2:g.127978A=

Transcript Alleles

HGVS Amino-acid change
ENST00000343533.10:c.3394A= (ATP7A) ENSP00000343026.6:p.Lys1132=
ENST00000682475.1:n.1781A= (ATP7A)
ENST00000685033.1:c.628A= (ATP7A) ENSP00000509269.1:p.Lys210=
ENST00000685264.1:c.3364A= (ATP7A) ENSP00000510136.1:p.Lys1122=
ENST00000686033.1:c.3169A= (ATP7A) ENSP00000510693.1:p.Lys1057=
ENST00000686133.1:c.3364A= (ATP7A) ENSP00000509233.1:p.Lys1122=
ENST00000686255.1:n.2395A= (ATP7A)
ENST00000686543.1:c.3130A= (ATP7A) ENSP00000509477.1:p.Lys1044=
ENST00000687086.1:c.3364A= (ATP7A) ENSP00000509566.1:p.Lys1122=
ENST00000689514.1:n.1406A= (ATP7A)
ENST00000689767.1:c.3457A= (ATP7A) ENSP00000509406.1:p.Lys1153=
ENST00000692908.1:c.3130A= (ATP7A) ENSP00000508627.1:p.Lys1044=
ENST00000341514.11:c.3364A= (ATP7A) MANE Select ENSP00000345728.6:p.Lys1122=
ENST00000644362.1:c.-19-76193A= (PGK1) ENSP00000496140.1:n.-19-76193A=
ENST00000645094.1:c.*3278A= (ATP7A) ENSP00000493605.1:n.*3278A=
ENST00000341514.10:c.3364A= (ATP7A) ENSP00000345728.6:p.Lys1122=
ENST00000343533.9:c.3130A= (ATP7A) ENSP00000343026.5:p.Lys1044=
ENST00000350425.5:c.*2537A= (ATP7A) ENSP00000343678.5:n.*2537A=
NM_000052.6:c.3364A= (ATP7A) NP_000043.4:p.Lys1122=
NM_001282224.1:c.3130A= (ATP7A) NP_001269153.1:p.Lys1044=
NR_104109.1:n.574A= (ATP7A)
NM_000052.7:c.3364A= (ATP7A) MANE Select NP_000043.4:p.Lys1122=
NR_104109.2:n.537A= (ATP7A)
NM_001282224.2:c.3130A= (ATP7A) NP_001269153.1:p.Lys1044=