Canonical Allele Identifier: CA277023

Linked Data

ClinVar Variation Id: 210454
ClinVar RCV Id: RCV000192813
dbSNP Id: rs797045379

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.78033812C>T , CM000685.2:g.78033812C>T GRCh38
NC_000023.10:g.77289310C>T , CM000685.1:g.77289310C>T GRCh37
NC_000023.9:g.77175966C>T NCBI36
NG_013224.2:g.128116C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000343533.10:c.3532C>T (ATP7A) ENSP00000343026.6:p.Gln1178Ter
ENST00000682475.1:n.1919C>T (ATP7A)
ENST00000685033.1:c.766C>T (ATP7A) ENSP00000509269.1:p.Gln256Ter
ENST00000685264.1:c.3502C>T (ATP7A) ENSP00000510136.1:p.Gln1168Ter
ENST00000686033.1:c.3307C>T (ATP7A) ENSP00000510693.1:p.Gln1103Ter
ENST00000686133.1:c.3502C>T (ATP7A) ENSP00000509233.1:p.Gln1168Ter
ENST00000686255.1:n.2533C>T (ATP7A)
ENST00000686543.1:c.3268C>T (ATP7A) ENSP00000509477.1:p.Gln1090Ter
ENST00000687086.1:c.3502C>T (ATP7A) ENSP00000509566.1:p.Gln1168Ter
ENST00000689514.1:n.1544C>T (ATP7A)
ENST00000689767.1:c.3595C>T (ATP7A) ENSP00000509406.1:p.Gln1199Ter
ENST00000692908.1:c.3268C>T (ATP7A) ENSP00000508627.1:p.Gln1090Ter
ENST00000341514.11:c.3502C>T (ATP7A) MANE Select ENSP00000345728.6:p.Gln1168Ter
ENST00000644362.1:c.-19-76055C>T (PGK1) ENSP00000496140.1:n.-19-76055C>T
ENST00000645094.1:c.*3416C>T (ATP7A) ENSP00000493605.1:n.*3416C>T
ENST00000341514.10:c.3502C>T (ATP7A) ENSP00000345728.6:p.Gln1168Ter
ENST00000343533.9:c.3268C>T (ATP7A) ENSP00000343026.5:p.Gln1090Ter
ENST00000350425.5:c.*2675C>T (ATP7A) ENSP00000343678.5:n.*2675C>T
NM_000052.6:c.3502C>T (ATP7A) NP_000043.4:p.Gln1168Ter
NM_001282224.1:c.3268C>T (ATP7A) NP_001269153.1:p.Gln1090Ter
NR_104109.1:n.712C>T (ATP7A)
NM_000052.7:c.3502C>T (ATP7A) MANE Select NP_000043.4:p.Gln1168Ter
NR_104109.2:n.675C>T (ATP7A)
NM_001282224.2:c.3268C>T (ATP7A) NP_001269153.1:p.Gln1090Ter