Canonical Allele Identifier: CA2439110485

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.78042694A= , CM000685.2:g.78042694A= GRCh38
NC_000023.10:g.77298192A= , CM000685.1:g.77298192A= GRCh37
NC_000023.9:g.77184848A= NCBI36
NG_013224.2:g.136998A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000343533.10:c.3941A= (ATP7A) ENSP00000343026.6:p.Asn1314=
ENST00000682475.1:n.2328A= (ATP7A)
ENST00000685033.1:c.1175A= (ATP7A) ENSP00000509269.1:p.Asn392=
ENST00000685264.1:c.3911A= (ATP7A) ENSP00000510136.1:p.Asn1304=
ENST00000686033.1:c.3716A= (ATP7A) ENSP00000510693.1:p.Asn1239=
ENST00000686133.1:c.3911A= (ATP7A) ENSP00000509233.1:p.Asn1304=
ENST00000686255.1:n.2942A= (ATP7A)
ENST00000686543.1:c.3677A= (ATP7A) ENSP00000509477.1:p.Asn1226=
ENST00000687086.1:c.3911A= (ATP7A) ENSP00000509566.1:p.Asn1304=
ENST00000689514.1:n.1953A= (ATP7A)
ENST00000689767.1:c.4004A= (ATP7A) ENSP00000509406.1:p.Asn1335=
ENST00000692908.1:c.3677A= (ATP7A) ENSP00000508627.1:p.Asn1226=
ENST00000341514.11:c.3911A= (ATP7A) MANE Select ENSP00000345728.6:p.Asn1304=
ENST00000644362.1:c.-19-67173A= (PGK1) ENSP00000496140.1:n.-19-67173A=
ENST00000341514.10:c.3911A= (ATP7A) ENSP00000345728.6:p.Asn1304=
ENST00000343533.9:c.3677A= (ATP7A) ENSP00000343026.5:p.Asn1226=
ENST00000350425.5:c.*3084A= (ATP7A) ENSP00000343678.5:n.*3084A=
NM_000052.6:c.3911A= (ATP7A) NP_000043.4:p.Asn1304=
NM_001282224.1:c.3677A= (ATP7A) NP_001269153.1:p.Asn1226=
NR_104109.1:n.1121A= (ATP7A)
NM_000052.7:c.3911A= (ATP7A) MANE Select NP_000043.4:p.Asn1304=
NR_104109.2:n.1084A= (ATP7A)
NM_001282224.2:c.3677A= (ATP7A) NP_001269153.1:p.Asn1226=