Canonical Allele Identifier: CA413606259
Community Standard Title: NM_000052.7(ATP7A):c.4363C>T (p.Arg1455Trp)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.78046430C>T , CM000685.2:g.78046430C>T GRCh38
NC_000023.10:g.77301927C>T , CM000685.1:g.77301927C>T GRCh37
NC_000023.9:g.77188583C>T NCBI36
NG_013224.2:g.140734C>T

Transcript Alleles

HGVS Amino-acid Change
NM_000052.7:c.4363C>T (ATP7A) MANE Select NP_000043.4:p.Arg1455Trp
ENST00000341514.11:c.4363C>T (ATP7A) MANE Select ENSP00000345728.6:p.Arg1455Trp
NM_000052.6:c.4363C>T (ATP7A) NP_000043.4:p.Arg1455Trp
NM_001282224.1:c.4129C>T (ATP7A) NP_001269153.1:p.Arg1377Trp
NM_001282224.2:c.4129C>T (ATP7A) NP_001269153.1:p.Arg1377Trp
NR_104109.1:n.1573C>T (ATP7A)
NR_104109.2:n.1536C>T (ATP7A)
ENST00000341514.10:c.4363C>T (ATP7A) ENSP00000345728.6:p.Arg1455Trp
ENST00000343533.10:c.4393C>T (ATP7A) ENSP00000343026.6:p.Arg1465Trp
ENST00000343533.9:c.4129C>T (ATP7A) ENSP00000343026.5:p.Arg1377Trp
ENST00000350425.5:c.*3536C>T (ATP7A) ENSP00000343678.5:n.*3536C>T
ENST00000644362.1:c.-19-63437C>T (PGK1) ENSP00000496140.1:n.-19-63437C>T
ENST00000682475.1:n.2780C>T (ATP7A)
ENST00000685033.1:c.1627C>T (ATP7A) ENSP00000509269.1:p.Arg543Trp
ENST00000685264.1:c.4363C>T (ATP7A) ENSP00000510136.1:p.Arg1455Trp
ENST00000686033.1:c.4168C>T (ATP7A) ENSP00000510693.1:p.Arg1390Trp
ENST00000686133.1:c.4363C>T (ATP7A) ENSP00000509233.1:p.Arg1455Trp
ENST00000686255.1:n.3394C>T (ATP7A)
ENST00000686543.1:c.4129C>T (ATP7A) ENSP00000509477.1:p.Arg1377Trp
ENST00000687086.1:c.4363C>T (ATP7A) ENSP00000509566.1:p.Arg1455Trp
ENST00000689083.1:n.1658C>T (ATP7A)
ENST00000689767.1:c.4456C>T (ATP7A) ENSP00000509406.1:p.Arg1486Trp
ENST00000692908.1:c.4129C>T (ATP7A) ENSP00000508627.1:p.Arg1377Trp