Canonical Allele Identifier: CA413606175
Community Standard Title: NM_000052.7(ATP7A):c.4323T>G (p.Asp1441Glu)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.78046390T>G , CM000685.2:g.78046390T>G GRCh38
NC_000023.10:g.77301887T>G , CM000685.1:g.77301887T>G GRCh37
NC_000023.9:g.77188543T>G NCBI36
NG_013224.2:g.140694T>G

Transcript Alleles

HGVS Amino-acid Change
NM_000052.7:c.4323T>G (ATP7A) MANE Select NP_000043.4:p.Asp1441Glu
ENST00000341514.11:c.4323T>G (ATP7A) MANE Select ENSP00000345728.6:p.Asp1441Glu
NM_000052.6:c.4323T>G (ATP7A) NP_000043.4:p.Asp1441Glu
NM_001282224.1:c.4089T>G (ATP7A) NP_001269153.1:p.Asp1363Glu
NM_001282224.2:c.4089T>G (ATP7A) NP_001269153.1:p.Asp1363Glu
NR_104109.1:n.1533T>G (ATP7A)
NR_104109.2:n.1496T>G (ATP7A)
ENST00000341514.10:c.4323T>G (ATP7A) ENSP00000345728.6:p.Asp1441Glu
ENST00000343533.10:c.4353T>G (ATP7A) ENSP00000343026.6:p.Asp1451Glu
ENST00000343533.9:c.4089T>G (ATP7A) ENSP00000343026.5:p.Asp1363Glu
ENST00000350425.5:c.*3496T>G (ATP7A) ENSP00000343678.5:n.*3496T>G
ENST00000644362.1:c.-19-63477T>G (PGK1) ENSP00000496140.1:n.-19-63477T>G
ENST00000682475.1:n.2740T>G (ATP7A)
ENST00000685033.1:c.1587T>G (ATP7A) ENSP00000509269.1:p.Asp529Glu
ENST00000685264.1:c.4323T>G (ATP7A) ENSP00000510136.1:p.Asp1441Glu
ENST00000686033.1:c.4128T>G (ATP7A) ENSP00000510693.1:p.Asp1376Glu
ENST00000686133.1:c.4323T>G (ATP7A) ENSP00000509233.1:p.Asp1441Glu
ENST00000686255.1:n.3354T>G (ATP7A)
ENST00000686543.1:c.4089T>G (ATP7A) ENSP00000509477.1:p.Asp1363Glu
ENST00000687086.1:c.4323T>G (ATP7A) ENSP00000509566.1:p.Asp1441Glu
ENST00000689083.1:n.1618T>G (ATP7A)
ENST00000689767.1:c.4416T>G (ATP7A) ENSP00000509406.1:p.Asp1472Glu
ENST00000692908.1:c.4089T>G (ATP7A) ENSP00000508627.1:p.Asp1363Glu