Canonical Allele Identifier: CA277221

Gene: ATP7A PGK1

Linked Data

• ClinVar Variation Id: 210415
• ClinVar RCV Id: RCV000193917 ; RCV001044291
• dbSNP Id: rs797045347
• MyVariant Identifiers: chrX:g.77267176G>C (hg19) ; chrX:g.78011679G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.78011679G>C , CM000685.2:g.78011679G>C	GRCh38
NC_000023.10:g.77267176G>C , CM000685.1:g.77267176G>C	GRCh37
NC_000023.9:g.77153832G>C	NCBI36
NG_013224.2:g.105983G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343533.10:c.2202+5G>C (ATP7A)	ENSP00000343026.6:n.2202+5G>C
ENST00000682475.1:n.823+5G>C (ATP7A)
ENST00000685264.1:c.2172+5G>C (ATP7A)	ENSP00000510136.1:n.2172+5G>C
ENST00000686033.1:c.2172+5G>C (ATP7A)	ENSP00000510693.1:n.2172+5G>C
ENST00000686133.1:c.2172+5G>C (ATP7A)	ENSP00000509233.1:n.2172+5G>C
ENST00000686255.1:n.1203+5G>C (ATP7A)
ENST00000686480.1:c.2172+5G>C (ATP7A)	ENSP00000508978.1:n.2172+5G>C
ENST00000686515.1:n.2312+5G>C (ATP7A)
ENST00000686543.1:c.2172+5G>C (ATP7A)	ENSP00000509477.1:n.2172+5G>C
ENST00000686688.1:c.2172+5G>C (ATP7A)	ENSP00000509416.1:n.2172+5G>C
ENST00000686999.1:n.2488G>C (ATP7A)
ENST00000687086.1:c.2172+5G>C (ATP7A)	ENSP00000509566.1:n.2172+5G>C
ENST00000687628.1:n.4386G>C (ATP7A)
ENST00000688746.1:n.2329G>C (ATP7A)
ENST00000689514.1:n.214+5G>C (ATP7A)
ENST00000689530.1:c.2172+5G>C (ATP7A)	ENSP00000509707.1:n.2172+5G>C
ENST00000689649.1:c.2172+5G>C (ATP7A)	ENSP00000509277.1:n.2172+5G>C
ENST00000689767.1:c.2265+5G>C (ATP7A)	ENSP00000509406.1:n.2265+5G>C
ENST00000689872.1:c.*121+5G>C (ATP7A)	ENSP00000509373.1:n.*121+5G>C
ENST00000692908.1:c.2172+5G>C (ATP7A)	ENSP00000508627.1:n.2172+5G>C
ENST00000693398.1:c.2172+5G>C (ATP7A)	ENSP00000510089.1:n.2172+5G>C
ENST00000341514.11:c.2172+5G>C (ATP7A) MANE Select	ENSP00000345728.6:n.2172+5G>C
ENST00000644362.1:c.-19-98188G>C (PGK1)	ENSP00000496140.1:n.-19-98188G>C
ENST00000645094.1:c.*2086+5G>C (ATP7A)	ENSP00000493605.1:n.*2086+5G>C
ENST00000341514.10:c.2172+5G>C (ATP7A)	ENSP00000345728.6:n.2172+5G>C
ENST00000343533.9:c.2172+5G>C (ATP7A)	ENSP00000343026.5:n.2172+5G>C
ENST00000350425.5:c.*1345+5G>C (ATP7A)	ENSP00000343678.5:n.*1345+5G>C
NM_000052.6:c.2172+5G>C (ATP7A)	NP_000043.4:n.2172+5G>C
NM_001282224.1:c.2172+5G>C (ATP7A)	NP_001269153.1:n.2172+5G>C
NR_104109.1:n.322-19721G>C (ATP7A)
NM_000052.7:c.2172+5G>C (ATP7A) MANE Select	NP_000043.4:n.2172+5G>C
NR_104109.2:n.285-19721G>C (ATP7A)
NM_001282224.2:c.2172+5G>C (ATP7A)	NP_001269153.1:n.2172+5G>C