Canonical Allele Identifier: CA2439099642

Gene: ATP7A PGK1

Linked Data

• dbSNP Id: rs2077800612

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.78009302_78009305del , CM000685.2:g.78009302_78009305del	GRCh38
NC_000023.10:g.77264799_77264802del , CM000685.1:g.77264799_77264802del	GRCh37
NC_000023.9:g.77151455_77151458del	NCBI36
NG_013224.2:g.103606_103609del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343533.10:c.1899+39_1899+42del (ATP7A)	ENSP00000343026.6:n.1899+39_1899+42del
ENST00000682742.2:n.2070_2073del (ATP7A)
ENST00000685264.1:c.1869+39_1869+42del (ATP7A)	ENSP00000510136.1:n.1869+39_1869+42del
ENST00000685434.1:n.1942_1945del (ATP7A)
ENST00000686033.1:c.1869+39_1869+42del (ATP7A)	ENSP00000510693.1:n.1869+39_1869+42del
ENST00000686133.1:c.1869+39_1869+42del (ATP7A)	ENSP00000509233.1:n.1869+39_1869+42del
ENST00000686416.1:n.2262_2265del (ATP7A)
ENST00000686480.1:c.1869+39_1869+42del (ATP7A)	ENSP00000508978.1:n.1869+39_1869+42del
ENST00000686515.1:n.2009+39_2009+42del (ATP7A)
ENST00000686543.1:c.1869+39_1869+42del (ATP7A)	ENSP00000509477.1:n.1869+39_1869+42del
ENST00000686688.1:c.1869+39_1869+42del (ATP7A)	ENSP00000509416.1:n.1869+39_1869+42del
ENST00000686999.1:n.2180+39_2180+42del (ATP7A)
ENST00000687086.1:c.1869+39_1869+42del (ATP7A)	ENSP00000509566.1:n.1869+39_1869+42del
ENST00000687628.1:n.2009_2012del (ATP7A)
ENST00000688746.1:n.2021+39_2021+42del (ATP7A)
ENST00000689530.1:c.1869+39_1869+42del (ATP7A)	ENSP00000509707.1:n.1869+39_1869+42del
ENST00000689541.1:n.2217_2220del (ATP7A)
ENST00000689649.1:c.1869+39_1869+42del (ATP7A)	ENSP00000509277.1:n.1869+39_1869+42del
ENST00000689767.1:c.1962+39_1962+42del (ATP7A)	ENSP00000509406.1:n.1962+39_1962+42del
ENST00000689872.1:c.1869+39_1869+42del (ATP7A)	ENSP00000509373.1:n.1869+39_1869+42del
ENST00000692110.1:c.1785+39_1785+42del (ATP7A)	ENSP00000509366.1:n.1785+39_1785+42del
ENST00000692908.1:c.1869+39_1869+42del (ATP7A)	ENSP00000508627.1:n.1869+39_1869+42del
ENST00000693387.1:c.*1837_*1840del (ATP7A)	ENSP00000508732.1:n.*1837_*1840del
ENST00000693398.1:c.1869+39_1869+42del (ATP7A)	ENSP00000510089.1:n.1869+39_1869+42del
ENST00000341514.11:c.1869+39_1869+42del (ATP7A) MANE Select	ENSP00000345728.6:n.1869+39_1869+42del
ENST00000644362.1:c.-20+98467_-20+98470del (PGK1)	ENSP00000496140.1:n.-20+98467_-20+98470del
ENST00000645094.1:c.*1783+39_*1783+42del (ATP7A)	ENSP00000493605.1:n.*1783+39_*1783+42del
ENST00000341514.10:c.1869+39_1869+42del (ATP7A)	ENSP00000345728.6:n.1869+39_1869+42del
ENST00000343533.9:c.1869+39_1869+42del (ATP7A)	ENSP00000343026.5:n.1869+39_1869+42del
ENST00000350425.5:c.*1042+39_*1042+42del (ATP7A)	ENSP00000343678.5:n.*1042+39_*1042+42del
NM_000052.6:c.1869+39_1869+42del (ATP7A)	NP_000043.4:n.1869+39_1869+42del
NM_001282224.1:c.1869+39_1869+42del (ATP7A)	NP_001269153.1:n.1869+39_1869+42del
NR_104109.1:n.322-22098_322-22095del (ATP7A)
NM_000052.7:c.1869+39_1869+42del (ATP7A) MANE Select	NP_000043.4:n.1869+39_1869+42del
NR_104109.2:n.285-22098_285-22095del (ATP7A)
NM_001282224.2:c.1869+39_1869+42del (ATP7A)	NP_001269153.1:n.1869+39_1869+42del