Canonical Allele Identifier: CA2439111617
Community Standard Title: NM_000052.7(ATP7A):c.4324G= (p.Asp1442=)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.78046391G= , CM000685.2:g.78046391G= GRCh38
NC_000023.10:g.77301888G= , CM000685.1:g.77301888G= GRCh37
NC_000023.9:g.77188544G= NCBI36
NG_013224.2:g.140695G=

Transcript Alleles

HGVS Amino-acid Change
NM_000052.7:c.4324G= (ATP7A) MANE Select NP_000043.4:p.Asp1442=
ENST00000341514.11:c.4324G= (ATP7A) MANE Select ENSP00000345728.6:p.Asp1442=
NM_000052.6:c.4324G= (ATP7A) NP_000043.4:p.Asp1442=
NM_001282224.1:c.4090G= (ATP7A) NP_001269153.1:p.Asp1364=
NM_001282224.2:c.4090G= (ATP7A) NP_001269153.1:p.Asp1364=
NR_104109.1:n.1534G= (ATP7A)
NR_104109.2:n.1497G= (ATP7A)
ENST00000341514.10:c.4324G= (ATP7A) ENSP00000345728.6:p.Asp1442=
ENST00000343533.10:c.4354G= (ATP7A) ENSP00000343026.6:p.Asp1452=
ENST00000343533.9:c.4090G= (ATP7A) ENSP00000343026.5:p.Asp1364=
ENST00000350425.5:c.*3497G= (ATP7A) ENSP00000343678.5:n.*3497G=
ENST00000644362.1:c.-19-63476G= (PGK1) ENSP00000496140.1:n.-19-63476G=
ENST00000682475.1:n.2741G= (ATP7A)
ENST00000685033.1:c.1588G= (ATP7A) ENSP00000509269.1:p.Asp530=
ENST00000685264.1:c.4324G= (ATP7A) ENSP00000510136.1:p.Asp1442=
ENST00000686033.1:c.4129G= (ATP7A) ENSP00000510693.1:p.Asp1377=
ENST00000686133.1:c.4324G= (ATP7A) ENSP00000509233.1:p.Asp1442=
ENST00000686255.1:n.3355G= (ATP7A)
ENST00000686543.1:c.4090G= (ATP7A) ENSP00000509477.1:p.Asp1364=
ENST00000687086.1:c.4324G= (ATP7A) ENSP00000509566.1:p.Asp1442=
ENST00000689083.1:n.1619G= (ATP7A)
ENST00000689767.1:c.4417G= (ATP7A) ENSP00000509406.1:p.Asp1473=
ENST00000692908.1:c.4090G= (ATP7A) ENSP00000508627.1:p.Asp1364=