Canonical Allele Identifier: CA517065483

Gene: ATP7A PGK1

Linked Data

• MyVariant Identifiers: chrX:g.77276567C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.78021070C>A , CM000685.2:g.78021070C>A	GRCh38
NC_000023.10:g.77276567C>A , CM000685.1:g.77276567C>A	GRCh37
NC_000023.9:g.77163223C>A	NCBI36
NG_013224.2:g.115374C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000343533.10:c.2937C>A (ATP7A)	ENSP00000343026.6:p.Thr979=
ENST00000682475.1:n.1324C>A (ATP7A)
ENST00000685033.1:c.375+672C>A (ATP7A)	ENSP00000509269.1:n.375+672C>A
ENST00000685264.1:c.2907C>A (ATP7A)	ENSP00000510136.1:p.Thr969=
ENST00000686033.1:c.2907C>A (ATP7A)	ENSP00000510693.1:p.Thr969=
ENST00000686133.1:c.2907C>A (ATP7A)	ENSP00000509233.1:p.Thr969=
ENST00000686255.1:n.1938C>A (ATP7A)
ENST00000686543.1:c.2673C>A (ATP7A)	ENSP00000509477.1:p.Thr891=
ENST00000687086.1:c.2907C>A (ATP7A)	ENSP00000509566.1:p.Thr969=
ENST00000689514.1:n.949C>A (ATP7A)
ENST00000689530.1:c.2907C>A (ATP7A)	ENSP00000509707.1:p.Thr969=
ENST00000689767.1:c.3000C>A (ATP7A)	ENSP00000509406.1:p.Thr1000=
ENST00000692908.1:c.2673C>A (ATP7A)	ENSP00000508627.1:p.Thr891=
ENST00000341514.11:c.2907C>A (ATP7A) MANE Select	ENSP00000345728.6:p.Thr969=
ENST00000644362.1:c.-19-88797C>A (PGK1)	ENSP00000496140.1:n.-19-88797C>A
ENST00000645094.1:c.*2821C>A (ATP7A)	ENSP00000493605.1:n.*2821C>A
ENST00000341514.10:c.2907C>A (ATP7A)	ENSP00000345728.6:p.Thr969=
ENST00000343533.9:c.2673C>A (ATP7A)	ENSP00000343026.5:p.Thr891=
ENST00000350425.5:c.*2080C>A (ATP7A)	ENSP00000343678.5:n.*2080C>A
NM_000052.6:c.2907C>A (ATP7A)	NP_000043.4:p.Thr969=
NM_001282224.1:c.2673C>A (ATP7A)	NP_001269153.1:p.Thr891=
NR_104109.1:n.322-10330C>A (ATP7A)
NM_000052.7:c.2907C>A (ATP7A) MANE Select	NP_000043.4:p.Thr969=
NR_104109.2:n.285-10330C>A (ATP7A)
NM_001282224.2:c.2673C>A (ATP7A)	NP_001269153.1:p.Thr891=