Canonical Allele Identifier: CA413603021
Community Standard Title: NM_000052.7(ATP7A):c.2924A>G (p.Asn975Ser)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.78029257A>G , CM000685.2:g.78029257A>G GRCh38
NC_000023.10:g.77284754A>G , CM000685.1:g.77284754A>G GRCh37
NC_000023.9:g.77171410A>G NCBI36
NG_013224.2:g.123561A>G

Transcript Alleles

HGVS Amino-acid Change
NM_000052.7:c.2924A>G (ATP7A) MANE Select NP_000043.4:p.Asn975Ser
ENST00000341514.11:c.2924A>G (ATP7A) MANE Select ENSP00000345728.6:p.Asn975Ser
NM_000052.6:c.2924A>G (ATP7A) NP_000043.4:p.Asn975Ser
NM_001282224.1:c.2690A>G (ATP7A) NP_001269153.1:p.Asn897Ser
NM_001282224.2:c.2690A>G (ATP7A) NP_001269153.1:p.Asn897Ser
NR_104109.1:n.322-2143A>G (ATP7A)
NR_104109.2:n.285-2143A>G (ATP7A)
ENST00000341514.10:c.2924A>G (ATP7A) ENSP00000345728.6:p.Asn975Ser
ENST00000343533.10:c.2954A>G (ATP7A) ENSP00000343026.6:p.Asn985Ser
ENST00000343533.9:c.2690A>G (ATP7A) ENSP00000343026.5:p.Asn897Ser
ENST00000350425.5:c.*2097A>G (ATP7A) ENSP00000343678.5:n.*2097A>G
ENST00000644362.1:c.-19-80610A>G (PGK1) ENSP00000496140.1:n.-19-80610A>G
ENST00000645094.1:c.*2838A>G (ATP7A) ENSP00000493605.1:n.*2838A>G
ENST00000682475.1:n.1341A>G (ATP7A)
ENST00000685033.1:c.376-2143A>G (ATP7A) ENSP00000509269.1:n.376-2143A>G
ENST00000685264.1:c.2924A>G (ATP7A) ENSP00000510136.1:p.Asn975Ser
ENST00000686033.1:c.2917-2143A>G (ATP7A) ENSP00000510693.1:n.2917-2143A>G
ENST00000686133.1:c.2924A>G (ATP7A) ENSP00000509233.1:p.Asn975Ser
ENST00000686255.1:n.1955A>G (ATP7A)
ENST00000686543.1:c.2690A>G (ATP7A) ENSP00000509477.1:p.Asn897Ser
ENST00000687086.1:c.2924A>G (ATP7A) ENSP00000509566.1:p.Asn975Ser
ENST00000689514.1:n.966A>G (ATP7A)
ENST00000689767.1:c.3017A>G (ATP7A) ENSP00000509406.1:p.Asn1006Ser
ENST00000692908.1:c.2690A>G (ATP7A) ENSP00000508627.1:p.Asn897Ser