Canonical Allele Identifier: CA413606169
Community Standard Title: NM_000052.7(ATP7A):c.4321G>T (p.Asp1441Tyr)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.78046388G>T , CM000685.2:g.78046388G>T GRCh38
NC_000023.10:g.77301885G>T , CM000685.1:g.77301885G>T GRCh37
NC_000023.9:g.77188541G>T NCBI36
NG_013224.2:g.140692G>T

Transcript Alleles

HGVS Amino-acid Change
NM_000052.7:c.4321G>T (ATP7A) MANE Select NP_000043.4:p.Asp1441Tyr
ENST00000341514.11:c.4321G>T (ATP7A) MANE Select ENSP00000345728.6:p.Asp1441Tyr
NM_000052.6:c.4321G>T (ATP7A) NP_000043.4:p.Asp1441Tyr
NM_001282224.1:c.4087G>T (ATP7A) NP_001269153.1:p.Asp1363Tyr
NM_001282224.2:c.4087G>T (ATP7A) NP_001269153.1:p.Asp1363Tyr
NR_104109.1:n.1531G>T (ATP7A)
NR_104109.2:n.1494G>T (ATP7A)
ENST00000341514.10:c.4321G>T (ATP7A) ENSP00000345728.6:p.Asp1441Tyr
ENST00000343533.10:c.4351G>T (ATP7A) ENSP00000343026.6:p.Asp1451Tyr
ENST00000343533.9:c.4087G>T (ATP7A) ENSP00000343026.5:p.Asp1363Tyr
ENST00000350425.5:c.*3494G>T (ATP7A) ENSP00000343678.5:n.*3494G>T
ENST00000644362.1:c.-19-63479G>T (PGK1) ENSP00000496140.1:n.-19-63479G>T
ENST00000682475.1:n.2738G>T (ATP7A)
ENST00000685033.1:c.1585G>T (ATP7A) ENSP00000509269.1:p.Asp529Tyr
ENST00000685264.1:c.4321G>T (ATP7A) ENSP00000510136.1:p.Asp1441Tyr
ENST00000686033.1:c.4126G>T (ATP7A) ENSP00000510693.1:p.Asp1376Tyr
ENST00000686133.1:c.4321G>T (ATP7A) ENSP00000509233.1:p.Asp1441Tyr
ENST00000686255.1:n.3352G>T (ATP7A)
ENST00000686543.1:c.4087G>T (ATP7A) ENSP00000509477.1:p.Asp1363Tyr
ENST00000687086.1:c.4321G>T (ATP7A) ENSP00000509566.1:p.Asp1441Tyr
ENST00000689083.1:n.1616G>T (ATP7A)
ENST00000689767.1:c.4414G>T (ATP7A) ENSP00000509406.1:p.Asp1472Tyr
ENST00000692908.1:c.4087G>T (ATP7A) ENSP00000508627.1:p.Asp1363Tyr