Canonical Allele Identifier: CA2439107663

Gene: ATP7A PGK1

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.78033797A= , CM000685.2:g.78033797A=	GRCh38
NC_000023.10:g.77289295A= , CM000685.1:g.77289295A=	GRCh37
NC_000023.9:g.77175951A=	NCBI36
NG_013224.2:g.128101A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343533.10:c.3517A= (ATP7A)	ENSP00000343026.6:p.Met1173=
ENST00000682475.1:n.1904A= (ATP7A)
ENST00000685033.1:c.751A= (ATP7A)	ENSP00000509269.1:p.Met251=
ENST00000685264.1:c.3487A= (ATP7A)	ENSP00000510136.1:p.Met1163=
ENST00000686033.1:c.3292A= (ATP7A)	ENSP00000510693.1:p.Met1098=
ENST00000686133.1:c.3487A= (ATP7A)	ENSP00000509233.1:p.Met1163=
ENST00000686255.1:n.2518A= (ATP7A)
ENST00000686543.1:c.3253A= (ATP7A)	ENSP00000509477.1:p.Met1085=
ENST00000687086.1:c.3487A= (ATP7A)	ENSP00000509566.1:p.Met1163=
ENST00000689514.1:n.1529A= (ATP7A)
ENST00000689767.1:c.3580A= (ATP7A)	ENSP00000509406.1:p.Met1194=
ENST00000692908.1:c.3253A= (ATP7A)	ENSP00000508627.1:p.Met1085=
ENST00000341514.11:c.3487A= (ATP7A) MANE Select	ENSP00000345728.6:p.Met1163=
ENST00000644362.1:c.-19-76070A= (PGK1)	ENSP00000496140.1:n.-19-76070A=
ENST00000645094.1:c.*3401A= (ATP7A)	ENSP00000493605.1:n.*3401A=
ENST00000341514.10:c.3487A= (ATP7A)	ENSP00000345728.6:p.Met1163=
ENST00000343533.9:c.3253A= (ATP7A)	ENSP00000343026.5:p.Met1085=
ENST00000350425.5:c.*2660A= (ATP7A)	ENSP00000343678.5:n.*2660A=
NM_000052.6:c.3487A= (ATP7A)	NP_000043.4:p.Met1163=
NM_001282224.1:c.3253A= (ATP7A)	NP_001269153.1:p.Met1085=
NR_104109.1:n.697A= (ATP7A)
NM_000052.7:c.3487A= (ATP7A) MANE Select	NP_000043.4:p.Met1163=
NR_104109.2:n.660A= (ATP7A)
NM_001282224.2:c.3253A= (ATP7A)	NP_001269153.1:p.Met1085=