Canonical Allele Identifier: CA277059

Linked Data

ClinVar Variation Id: 210417
ClinVar RCV Id: RCV000192993
dbSNP Id: rs797045349

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.78012877A>G , CM000685.2:g.78012877A>G GRCh38
NC_000023.10:g.77268374A>G , CM000685.1:g.77268374A>G GRCh37
NC_000023.9:g.77155030A>G NCBI36
NG_013224.2:g.107181A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000343533.10:c.2203-2A>G (ATP7A) ENSP00000343026.6:n.2203-2A>G
ENST00000682475.1:n.823+1203A>G (ATP7A)
ENST00000685264.1:c.2173-2A>G (ATP7A) ENSP00000510136.1:n.2173-2A>G
ENST00000686033.1:c.2173-2A>G (ATP7A) ENSP00000510693.1:n.2173-2A>G
ENST00000686133.1:c.2173-2A>G (ATP7A) ENSP00000509233.1:n.2173-2A>G
ENST00000686255.1:n.1204-2A>G (ATP7A)
ENST00000686480.1:c.2172+1203A>G (ATP7A) ENSP00000508978.1:n.2172+1203A>G
ENST00000686543.1:c.2172+1203A>G (ATP7A) ENSP00000509477.1:n.2172+1203A>G
ENST00000686688.1:c.2173-2A>G (ATP7A) ENSP00000509416.1:n.2173-2A>G
ENST00000687086.1:c.2173-2A>G (ATP7A) ENSP00000509566.1:n.2173-2A>G
ENST00000688746.1:n.3527A>G (ATP7A)
ENST00000689514.1:n.215-2A>G (ATP7A)
ENST00000689530.1:c.2173-2A>G (ATP7A) ENSP00000509707.1:n.2173-2A>G
ENST00000689649.1:c.2173-2A>G (ATP7A) ENSP00000509277.1:n.2173-2A>G
ENST00000689767.1:c.2266-2A>G (ATP7A) ENSP00000509406.1:n.2266-2A>G
ENST00000689872.1:c.*122-2A>G (ATP7A) ENSP00000509373.1:n.*122-2A>G
ENST00000692908.1:c.2172+1203A>G (ATP7A) ENSP00000508627.1:n.2172+1203A>G
ENST00000693398.1:c.2173-2A>G (ATP7A) ENSP00000510089.1:n.2173-2A>G
ENST00000341514.11:c.2173-2A>G (ATP7A) MANE Select ENSP00000345728.6:n.2173-2A>G
ENST00000644362.1:c.-19-96990A>G (PGK1) ENSP00000496140.1:n.-19-96990A>G
ENST00000645094.1:c.*2087-2A>G (ATP7A) ENSP00000493605.1:n.*2087-2A>G
ENST00000341514.10:c.2173-2A>G (ATP7A) ENSP00000345728.6:n.2173-2A>G
ENST00000343533.9:c.2172+1203A>G (ATP7A) ENSP00000343026.5:n.2172+1203A>G
ENST00000350425.5:c.*1346-2A>G (ATP7A) ENSP00000343678.5:n.*1346-2A>G
NM_000052.6:c.2173-2A>G (ATP7A) NP_000043.4:n.2173-2A>G
NM_001282224.1:c.2172+1203A>G (ATP7A) NP_001269153.1:n.2172+1203A>G
NR_104109.1:n.322-18523A>G (ATP7A)
NM_000052.7:c.2173-2A>G (ATP7A) MANE Select NP_000043.4:n.2173-2A>G
NR_104109.2:n.285-18523A>G (ATP7A)
NM_001282224.2:c.2172+1203A>G (ATP7A) NP_001269153.1:n.2172+1203A>G