Canonical Allele Identifier: CA2439107615

Gene: ATP7A PGK1

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.78033614A= , CM000685.2:g.78033614A=	GRCh38
NC_000023.10:g.77289112A= , CM000685.1:g.77289112A=	GRCh37
NC_000023.9:g.77175768A=	NCBI36
NG_013224.2:g.127918A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343533.10:c.3334A= (ATP7A)	ENSP00000343026.6:p.Thr1112=
ENST00000682475.1:n.1721A= (ATP7A)
ENST00000685033.1:c.568A= (ATP7A)	ENSP00000509269.1:p.Thr190=
ENST00000685264.1:c.3304A= (ATP7A)	ENSP00000510136.1:p.Thr1102=
ENST00000686033.1:c.3109A= (ATP7A)	ENSP00000510693.1:p.Thr1037=
ENST00000686133.1:c.3304A= (ATP7A)	ENSP00000509233.1:p.Thr1102=
ENST00000686255.1:n.2335A= (ATP7A)
ENST00000686543.1:c.3070A= (ATP7A)	ENSP00000509477.1:p.Thr1024=
ENST00000687086.1:c.3304A= (ATP7A)	ENSP00000509566.1:p.Thr1102=
ENST00000689514.1:n.1346A= (ATP7A)
ENST00000689767.1:c.3397A= (ATP7A)	ENSP00000509406.1:p.Thr1133=
ENST00000692908.1:c.3070A= (ATP7A)	ENSP00000508627.1:p.Thr1024=
ENST00000341514.11:c.3304A= (ATP7A) MANE Select	ENSP00000345728.6:p.Thr1102=
ENST00000644362.1:c.-19-76253A= (PGK1)	ENSP00000496140.1:n.-19-76253A=
ENST00000645094.1:c.*3218A= (ATP7A)	ENSP00000493605.1:n.*3218A=
ENST00000341514.10:c.3304A= (ATP7A)	ENSP00000345728.6:p.Thr1102=
ENST00000343533.9:c.3070A= (ATP7A)	ENSP00000343026.5:p.Thr1024=
ENST00000350425.5:c.*2477A= (ATP7A)	ENSP00000343678.5:n.*2477A=
NM_000052.6:c.3304A= (ATP7A)	NP_000043.4:p.Thr1102=
NM_001282224.1:c.3070A= (ATP7A)	NP_001269153.1:p.Thr1024=
NR_104109.1:n.514A= (ATP7A)
NM_000052.7:c.3304A= (ATP7A) MANE Select	NP_000043.4:p.Thr1102=
NR_104109.2:n.477A= (ATP7A)
NM_001282224.2:c.3070A= (ATP7A)	NP_001269153.1:p.Thr1024=