Canonical Allele Identifier: CA413605808

Gene: ATP7A PGK1

Linked Data

• MyVariant Identifiers: chrX:g.77301003G>C (hg19) ; chrX:g.78045506G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.78045506G>C , CM000685.2:g.78045506G>C	GRCh38
NC_000023.10:g.77301003G>C , CM000685.1:g.77301003G>C	GRCh37
NC_000023.9:g.77187659G>C	NCBI36
NG_013224.2:g.139810G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000343533.10:c.4190G>C (ATP7A)	ENSP00000343026.6:p.Trp1397Ser
ENST00000682475.1:n.2577G>C (ATP7A)
ENST00000685033.1:c.1424G>C (ATP7A)	ENSP00000509269.1:p.Trp475Ser
ENST00000685264.1:c.4160G>C (ATP7A)	ENSP00000510136.1:p.Trp1387Ser
ENST00000686033.1:c.3965G>C (ATP7A)	ENSP00000510693.1:p.Trp1322Ser
ENST00000686133.1:c.4160G>C (ATP7A)	ENSP00000509233.1:p.Trp1387Ser
ENST00000686255.1:n.3191G>C (ATP7A)
ENST00000686543.1:c.3926G>C (ATP7A)	ENSP00000509477.1:p.Trp1309Ser
ENST00000687086.1:c.4160G>C (ATP7A)	ENSP00000509566.1:p.Trp1387Ser
ENST00000689083.1:n.1455G>C (ATP7A)
ENST00000689767.1:c.4253G>C (ATP7A)	ENSP00000509406.1:p.Trp1418Ser
ENST00000692908.1:c.3926G>C (ATP7A)	ENSP00000508627.1:p.Trp1309Ser
ENST00000341514.11:c.4160G>C (ATP7A) MANE Select	ENSP00000345728.6:p.Trp1387Ser
ENST00000644362.1:c.-19-64361G>C (PGK1)	ENSP00000496140.1:n.-19-64361G>C
ENST00000341514.10:c.4160G>C (ATP7A)	ENSP00000345728.6:p.Trp1387Ser
ENST00000343533.9:c.3926G>C (ATP7A)	ENSP00000343026.5:p.Trp1309Ser
ENST00000350425.5:c.*3333G>C (ATP7A)	ENSP00000343678.5:n.*3333G>C
NM_000052.6:c.4160G>C (ATP7A)	NP_000043.4:p.Trp1387Ser
NM_001282224.1:c.3926G>C (ATP7A)	NP_001269153.1:p.Trp1309Ser
NR_104109.1:n.1370G>C (ATP7A)
NM_000052.7:c.4160G>C (ATP7A) MANE Select	NP_000043.4:p.Trp1387Ser
NR_104109.2:n.1333G>C (ATP7A)
NM_001282224.2:c.3926G>C (ATP7A)	NP_001269153.1:p.Trp1309Ser