Canonical Allele Identifier: CA413604070

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.78033709T>G , CM000685.2:g.78033709T>G GRCh38
NC_000023.10:g.77289207T>G , CM000685.1:g.77289207T>G GRCh37
NC_000023.9:g.77175863T>G NCBI36
NG_013224.2:g.128013T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000343533.10:c.3429T>G (ATP7A) ENSP00000343026.6:p.Asn1143Lys
ENST00000682475.1:n.1816T>G (ATP7A)
ENST00000685033.1:c.663T>G (ATP7A) ENSP00000509269.1:p.Asn221Lys
ENST00000685264.1:c.3399T>G (ATP7A) ENSP00000510136.1:p.Asn1133Lys
ENST00000686033.1:c.3204T>G (ATP7A) ENSP00000510693.1:p.Asn1068Lys
ENST00000686133.1:c.3399T>G (ATP7A) ENSP00000509233.1:p.Asn1133Lys
ENST00000686255.1:n.2430T>G (ATP7A)
ENST00000686543.1:c.3165T>G (ATP7A) ENSP00000509477.1:p.Asn1055Lys
ENST00000687086.1:c.3399T>G (ATP7A) ENSP00000509566.1:p.Asn1133Lys
ENST00000689514.1:n.1441T>G (ATP7A)
ENST00000689767.1:c.3492T>G (ATP7A) ENSP00000509406.1:p.Asn1164Lys
ENST00000692908.1:c.3165T>G (ATP7A) ENSP00000508627.1:p.Asn1055Lys
ENST00000341514.11:c.3399T>G (ATP7A) MANE Select ENSP00000345728.6:p.Asn1133Lys
ENST00000644362.1:c.-19-76158T>G (PGK1) ENSP00000496140.1:n.-19-76158T>G
ENST00000645094.1:c.*3313T>G (ATP7A) ENSP00000493605.1:n.*3313T>G
ENST00000341514.10:c.3399T>G (ATP7A) ENSP00000345728.6:p.Asn1133Lys
ENST00000343533.9:c.3165T>G (ATP7A) ENSP00000343026.5:p.Asn1055Lys
ENST00000350425.5:c.*2572T>G (ATP7A) ENSP00000343678.5:n.*2572T>G
NM_000052.6:c.3399T>G (ATP7A) NP_000043.4:p.Asn1133Lys
NM_001282224.1:c.3165T>G (ATP7A) NP_001269153.1:p.Asn1055Lys
NR_104109.1:n.609T>G (ATP7A)
NM_000052.7:c.3399T>G (ATP7A) MANE Select NP_000043.4:p.Asn1133Lys
NR_104109.2:n.572T>G (ATP7A)
NM_001282224.2:c.3165T>G (ATP7A) NP_001269153.1:p.Asn1055Lys