Canonical Allele Identifier: CA878406036

Gene: ATP7A PGK1

Linked Data

• dbSNP Id: rs1188354826
• gnomAD v3: X-78033394-G-T
• gnomAD v4: X-78033394-G-T
• MyVariant Identifiers: chrX:g.78033394G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.78033394G>T , CM000685.2:g.78033394G>T	GRCh38
NC_000023.10:g.77288892G>T , CM000685.1:g.77288892G>T	GRCh37
NC_000023.9:g.77175548G>T	NCBI36
NG_013224.2:g.127698G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343533.10:c.3325-211G>T (ATP7A)	ENSP00000343026.6:n.3325-211G>T
ENST00000682475.1:n.1712-211G>T (ATP7A)
ENST00000685033.1:c.559-211G>T (ATP7A)	ENSP00000509269.1:n.559-211G>T
ENST00000685264.1:c.3295-211G>T (ATP7A)	ENSP00000510136.1:n.3295-211G>T
ENST00000686033.1:c.3100-211G>T (ATP7A)	ENSP00000510693.1:n.3100-211G>T
ENST00000686133.1:c.3295-211G>T (ATP7A)	ENSP00000509233.1:n.3295-211G>T
ENST00000686255.1:n.2326-211G>T (ATP7A)
ENST00000686543.1:c.3061-211G>T (ATP7A)	ENSP00000509477.1:n.3061-211G>T
ENST00000687086.1:c.3295-211G>T (ATP7A)	ENSP00000509566.1:n.3295-211G>T
ENST00000689514.1:n.1337-211G>T (ATP7A)
ENST00000689767.1:c.3388-211G>T (ATP7A)	ENSP00000509406.1:n.3388-211G>T
ENST00000692908.1:c.3061-211G>T (ATP7A)	ENSP00000508627.1:n.3061-211G>T
ENST00000341514.11:c.3295-211G>T (ATP7A) MANE Select	ENSP00000345728.6:n.3295-211G>T
ENST00000644362.1:c.-19-76473G>T (PGK1)	ENSP00000496140.1:n.-19-76473G>T
ENST00000645094.1:c.*3209-211G>T (ATP7A)	ENSP00000493605.1:n.*3209-211G>T
ENST00000341514.10:c.3295-211G>T (ATP7A)	ENSP00000345728.6:n.3295-211G>T
ENST00000343533.9:c.3061-211G>T (ATP7A)	ENSP00000343026.5:n.3061-211G>T
ENST00000350425.5:c.*2468-211G>T (ATP7A)	ENSP00000343678.5:n.*2468-211G>T
NM_000052.6:c.3295-211G>T (ATP7A)	NP_000043.4:n.3295-211G>T
NM_001282224.1:c.3061-211G>T (ATP7A)	NP_001269153.1:n.3061-211G>T
NR_104109.1:n.505-211G>T (ATP7A)
NM_000052.7:c.3295-211G>T (ATP7A) MANE Select	NP_000043.4:n.3295-211G>T
NR_104109.2:n.468-211G>T (ATP7A)
NM_001282224.2:c.3061-211G>T (ATP7A)	NP_001269153.1:n.3061-211G>T