Canonical Allele Identifier: CA2821937015

Gene: ATP7A PGK1

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.78009369_78009370insAGG , CM000685.2:g.78009369_78009370insAGG	GRCh38
NC_000023.10:g.77264866_77264867insAGG , CM000685.1:g.77264866_77264867insAGG	GRCh37
NC_000023.9:g.77151522_77151523insAGG	NCBI36
NG_013224.2:g.103673_103674insAGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343533.10:c.1899+106_1899+107insAGG (ATP7A)	ENSP00000343026.6:n.1899+106_1899+107insAGG
ENST00000685264.1:c.1869+106_1869+107insAGG (ATP7A)	ENSP00000510136.1:n.1869+106_1869+107insAGG
ENST00000686033.1:c.1869+106_1869+107insAGG (ATP7A)	ENSP00000510693.1:n.1869+106_1869+107insAGG
ENST00000686133.1:c.1869+106_1869+107insAGG (ATP7A)	ENSP00000509233.1:n.1869+106_1869+107insAGG
ENST00000686416.1:n.2329_2330insAGG (ATP7A)
ENST00000686480.1:c.1869+106_1869+107insAGG (ATP7A)	ENSP00000508978.1:n.1869+106_1869+107insAGG
ENST00000686515.1:n.2009+106_2009+107insAGG (ATP7A)
ENST00000686543.1:c.1869+106_1869+107insAGG (ATP7A)	ENSP00000509477.1:n.1869+106_1869+107insAGG
ENST00000686688.1:c.1869+106_1869+107insAGG (ATP7A)	ENSP00000509416.1:n.1869+106_1869+107insAGG
ENST00000686999.1:n.2180+106_2180+107insAGG (ATP7A)
ENST00000687086.1:c.1869+106_1869+107insAGG (ATP7A)	ENSP00000509566.1:n.1869+106_1869+107insAGG
ENST00000687628.1:n.2076_2077insAGG (ATP7A)
ENST00000688746.1:n.2021+106_2021+107insAGG (ATP7A)
ENST00000689530.1:c.1869+106_1869+107insAGG (ATP7A)	ENSP00000509707.1:n.1869+106_1869+107insAGG
ENST00000689541.1:n.2284_2285insAGG (ATP7A)
ENST00000689649.1:c.1869+106_1869+107insAGG (ATP7A)	ENSP00000509277.1:n.1869+106_1869+107insAGG
ENST00000689767.1:c.1962+106_1962+107insAGG (ATP7A)	ENSP00000509406.1:n.1962+106_1962+107insAGG
ENST00000689872.1:c.1869+106_1869+107insAGG (ATP7A)	ENSP00000509373.1:n.1869+106_1869+107insAGG
ENST00000692110.1:c.1785+106_1785+107insAGG (ATP7A)	ENSP00000509366.1:n.1785+106_1785+107insAGG
ENST00000692908.1:c.1869+106_1869+107insAGG (ATP7A)	ENSP00000508627.1:n.1869+106_1869+107insAGG
ENST00000693398.1:c.1869+106_1869+107insAGG (ATP7A)	ENSP00000510089.1:n.1869+106_1869+107insAGG
ENST00000341514.11:c.1869+106_1869+107insAGG (ATP7A) MANE Select	ENSP00000345728.6:n.1869+106_1869+107insAGG
ENST00000644362.1:c.-20+98534_-20+98535insAGG (PGK1)	ENSP00000496140.1:n.-20+98534_-20+98535insAGG
ENST00000645094.1:c.*1783+106_*1783+107insAGG (ATP7A)	ENSP00000493605.1:n.*1783+106_*1783+107insAGG
ENST00000341514.10:c.1869+106_1869+107insAGG (ATP7A)	ENSP00000345728.6:n.1869+106_1869+107insAGG
ENST00000343533.9:c.1869+106_1869+107insAGG (ATP7A)	ENSP00000343026.5:n.1869+106_1869+107insAGG
ENST00000350425.5:c.*1042+106_*1042+107insAGG (ATP7A)	ENSP00000343678.5:n.*1042+106_*1042+107insAGG
NM_000052.6:c.1869+106_1869+107insAGG (ATP7A)	NP_000043.4:n.1869+106_1869+107insAGG
NM_001282224.1:c.1869+106_1869+107insAGG (ATP7A)	NP_001269153.1:n.1869+106_1869+107insAGG
NR_104109.1:n.322-22031_322-22030insAGG (ATP7A)
NM_000052.7:c.1869+106_1869+107insAGG (ATP7A) MANE Select	NP_000043.4:n.1869+106_1869+107insAGG
NR_104109.2:n.285-22031_285-22030insAGG (ATP7A)
NM_001282224.2:c.1869+106_1869+107insAGG (ATP7A)	NP_001269153.1:n.1869+106_1869+107insAGG