Canonical Allele Identifier: CA277364

Linked Data

ClinVar Variation Id: 210450
ClinVar RCV Id: RCV000194716
dbSNP Id: rs797045376

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.78033662G>T , CM000685.2:g.78033662G>T GRCh38
NC_000023.10:g.77289160G>T , CM000685.1:g.77289160G>T GRCh37
NC_000023.9:g.77175816G>T NCBI36
NG_013224.2:g.127966G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000343533.10:c.3382G>T (ATP7A) ENSP00000343026.6:p.Gly1128Cys
ENST00000682475.1:n.1769G>T (ATP7A)
ENST00000685033.1:c.616G>T (ATP7A) ENSP00000509269.1:p.Gly206Cys
ENST00000685264.1:c.3352G>T (ATP7A) ENSP00000510136.1:p.Gly1118Cys
ENST00000686033.1:c.3157G>T (ATP7A) ENSP00000510693.1:p.Gly1053Cys
ENST00000686133.1:c.3352G>T (ATP7A) ENSP00000509233.1:p.Gly1118Cys
ENST00000686255.1:n.2383G>T (ATP7A)
ENST00000686543.1:c.3118G>T (ATP7A) ENSP00000509477.1:p.Gly1040Cys
ENST00000687086.1:c.3352G>T (ATP7A) ENSP00000509566.1:p.Gly1118Cys
ENST00000689514.1:n.1394G>T (ATP7A)
ENST00000689767.1:c.3445G>T (ATP7A) ENSP00000509406.1:p.Gly1149Cys
ENST00000692908.1:c.3118G>T (ATP7A) ENSP00000508627.1:p.Gly1040Cys
ENST00000341514.11:c.3352G>T (ATP7A) MANE Select ENSP00000345728.6:p.Gly1118Cys
ENST00000644362.1:c.-19-76205G>T (PGK1) ENSP00000496140.1:n.-19-76205G>T
ENST00000645094.1:c.*3266G>T (ATP7A) ENSP00000493605.1:n.*3266G>T
ENST00000341514.10:c.3352G>T (ATP7A) ENSP00000345728.6:p.Gly1118Cys
ENST00000343533.9:c.3118G>T (ATP7A) ENSP00000343026.5:p.Gly1040Cys
ENST00000350425.5:c.*2525G>T (ATP7A) ENSP00000343678.5:n.*2525G>T
NM_000052.6:c.3352G>T (ATP7A) NP_000043.4:p.Gly1118Cys
NM_001282224.1:c.3118G>T (ATP7A) NP_001269153.1:p.Gly1040Cys
NR_104109.1:n.562G>T (ATP7A)
NM_000052.7:c.3352G>T (ATP7A) MANE Select NP_000043.4:p.Gly1118Cys
NR_104109.2:n.525G>T (ATP7A)
NM_001282224.2:c.3118G>T (ATP7A) NP_001269153.1:p.Gly1040Cys