Canonical Allele Identifier: CA2694152508

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.78033537del , CM000685.2:g.78033537del GRCh38
NC_000023.10:g.77289035del , CM000685.1:g.77289035del GRCh37
NC_000023.9:g.77175691del NCBI36
NG_013224.2:g.127841del

Transcript Alleles

HGVS Amino-acid Change
ENST00000343533.10:c.3325-68del (ATP7A) ENSP00000343026.6:n.3325-68del
ENST00000682475.1:n.1712-68del (ATP7A)
ENST00000685033.1:c.559-68del (ATP7A) ENSP00000509269.1:n.559-68del
ENST00000685264.1:c.3295-68del (ATP7A) ENSP00000510136.1:n.3295-68del
ENST00000686033.1:c.3100-68del (ATP7A) ENSP00000510693.1:n.3100-68del
ENST00000686133.1:c.3295-68del (ATP7A) ENSP00000509233.1:n.3295-68del
ENST00000686255.1:n.2326-68del (ATP7A)
ENST00000686543.1:c.3061-68del (ATP7A) ENSP00000509477.1:n.3061-68del
ENST00000687086.1:c.3295-68del (ATP7A) ENSP00000509566.1:n.3295-68del
ENST00000689514.1:n.1337-68del (ATP7A)
ENST00000689767.1:c.3388-68del (ATP7A) ENSP00000509406.1:n.3388-68del
ENST00000692908.1:c.3061-68del (ATP7A) ENSP00000508627.1:n.3061-68del
ENST00000341514.11:c.3295-68del (ATP7A) MANE Select ENSP00000345728.6:n.3295-68del
ENST00000644362.1:c.-19-76330del (PGK1) ENSP00000496140.1:n.-19-76330del
ENST00000645094.1:c.*3209-68del (ATP7A) ENSP00000493605.1:n.*3209-68del
ENST00000341514.10:c.3295-68del (ATP7A) ENSP00000345728.6:n.3295-68del
ENST00000343533.9:c.3061-68del (ATP7A) ENSP00000343026.5:n.3061-68del
ENST00000350425.5:c.*2468-68del (ATP7A) ENSP00000343678.5:n.*2468-68del
NM_000052.6:c.3295-68del (ATP7A) NP_000043.4:n.3295-68del
NM_001282224.1:c.3061-68del (ATP7A) NP_001269153.1:n.3061-68del
NR_104109.1:n.505-68del (ATP7A)
NM_000052.7:c.3295-68del (ATP7A) MANE Select NP_000043.4:n.3295-68del
NR_104109.2:n.468-68del (ATP7A)
NM_001282224.2:c.3061-68del (ATP7A) NP_001269153.1:n.3061-68del