Canonical Allele Identifier: CA277176

Linked Data

ClinVar Variation Id: 210449
ClinVar RCV Id: RCV000193615
dbSNP Id: rs797045375

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.78033650del , CM000685.2:g.78033650del GRCh38
NC_000023.10:g.77289148del , CM000685.1:g.77289148del GRCh37
NC_000023.9:g.77175804del NCBI36
NG_013224.2:g.127954del

Transcript Alleles

HGVS Amino-acid change
ENST00000343533.10:c.3370del (ATP7A) ENSP00000343026.6:p.Val1124CysfsTer24
ENST00000682475.1:n.1757del (ATP7A)
ENST00000685033.1:c.604del (ATP7A) ENSP00000509269.1:p.Val202CysfsTer24
ENST00000685264.1:c.3340del (ATP7A) ENSP00000510136.1:p.Val1114CysfsTer24
ENST00000686033.1:c.3145del (ATP7A) ENSP00000510693.1:p.Val1049CysfsTer24
ENST00000686133.1:c.3340del (ATP7A) ENSP00000509233.1:p.Val1114CysfsTer24
ENST00000686255.1:n.2371del (ATP7A)
ENST00000686543.1:c.3106del (ATP7A) ENSP00000509477.1:p.Val1036CysfsTer24
ENST00000687086.1:c.3340del (ATP7A) ENSP00000509566.1:p.Val1114CysfsTer24
ENST00000689514.1:n.1382del (ATP7A)
ENST00000689767.1:c.3433del (ATP7A) ENSP00000509406.1:p.Val1145CysfsTer24
ENST00000692908.1:c.3106del (ATP7A) ENSP00000508627.1:p.Val1036CysfsTer24
ENST00000341514.11:c.3340del (ATP7A) MANE Select ENSP00000345728.6:p.Val1114CysfsTer24
ENST00000644362.1:c.-19-76217del (PGK1) ENSP00000496140.1:n.-19-76217del
ENST00000645094.1:c.*3254del (ATP7A) ENSP00000493605.1:n.*3254del
ENST00000341514.10:c.3340del (ATP7A) ENSP00000345728.6:p.Val1114CysfsTer24
ENST00000343533.9:c.3106del (ATP7A) ENSP00000343026.5:p.Val1036CysfsTer24
ENST00000350425.5:c.*2513del (ATP7A) ENSP00000343678.5:n.*2513del
NM_000052.6:c.3340del (ATP7A) NP_000043.4:p.Val1114CysfsTer24
NM_001282224.1:c.3106del (ATP7A) NP_001269153.1:p.Val1036CysfsTer24
NR_104109.1:n.550del (ATP7A)
NM_000052.7:c.3340del (ATP7A) MANE Select NP_000043.4:p.Val1114CysfsTer24
NR_104109.2:n.513del (ATP7A)
NM_001282224.2:c.3106del (ATP7A) NP_001269153.1:p.Val1036CysfsTer24