Canonical Allele Identifier: CA2821936928

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.78008842_78008843del , CM000685.2:g.78008842_78008843del GRCh38
NC_000023.10:g.77264339_77264340del , CM000685.1:g.77264339_77264340del GRCh37
NC_000023.9:g.77150995_77150996del NCBI36
NG_013224.2:g.103146_103147del

Transcript Alleles

HGVS Amino-acid Change
ENST00000343533.10:c.1738-260_1738-259del (ATP7A) ENSP00000343026.6:n.1738-260_1738-259del
ENST00000682742.2:n.1870-260_1870-259del (ATP7A)
ENST00000685264.1:c.1708-260_1708-259del (ATP7A) ENSP00000510136.1:n.1708-260_1708-259del
ENST00000685434.1:n.1742-260_1742-259del (ATP7A)
ENST00000686033.1:c.1708-260_1708-259del (ATP7A) ENSP00000510693.1:n.1708-260_1708-259del
ENST00000686133.1:c.1708-260_1708-259del (ATP7A) ENSP00000509233.1:n.1708-260_1708-259del
ENST00000686416.1:n.2062-260_2062-259del (ATP7A)
ENST00000686480.1:c.1708-260_1708-259del (ATP7A) ENSP00000508978.1:n.1708-260_1708-259del
ENST00000686515.1:n.1848-260_1848-259del (ATP7A)
ENST00000686543.1:c.1708-260_1708-259del (ATP7A) ENSP00000509477.1:n.1708-260_1708-259del
ENST00000686688.1:c.1708-260_1708-259del (ATP7A) ENSP00000509416.1:n.1708-260_1708-259del
ENST00000686999.1:n.2019-260_2019-259del (ATP7A)
ENST00000687086.1:c.1708-260_1708-259del (ATP7A) ENSP00000509566.1:n.1708-260_1708-259del
ENST00000687628.1:n.1809-260_1809-259del (ATP7A)
ENST00000688746.1:n.1860-260_1860-259del (ATP7A)
ENST00000689530.1:c.1708-260_1708-259del (ATP7A) ENSP00000509707.1:n.1708-260_1708-259del
ENST00000689541.1:n.2017-260_2017-259del (ATP7A)
ENST00000689649.1:c.1708-260_1708-259del (ATP7A) ENSP00000509277.1:n.1708-260_1708-259del
ENST00000689767.1:c.1801-260_1801-259del (ATP7A) ENSP00000509406.1:n.1801-260_1801-259del
ENST00000689872.1:c.1708-260_1708-259del (ATP7A) ENSP00000509373.1:n.1708-260_1708-259del
ENST00000692110.1:c.1624-260_1624-259del (ATP7A) ENSP00000509366.1:n.1624-260_1624-259del
ENST00000692908.1:c.1708-260_1708-259del (ATP7A) ENSP00000508627.1:n.1708-260_1708-259del
ENST00000693387.1:c.*1637-260_*1637-259del (ATP7A) ENSP00000508732.1:n.*1637-260_*1637-259del
ENST00000693398.1:c.1708-260_1708-259del (ATP7A) ENSP00000510089.1:n.1708-260_1708-259del
ENST00000341514.11:c.1708-260_1708-259del (ATP7A) MANE Select ENSP00000345728.6:n.1708-260_1708-259del
ENST00000644362.1:c.-20+98007_-20+98008del (PGK1) ENSP00000496140.1:n.-20+98007_-20+98008del
ENST00000645094.1:c.*1622-260_*1622-259del (ATP7A) ENSP00000493605.1:n.*1622-260_*1622-259del
ENST00000341514.10:c.1708-260_1708-259del (ATP7A) ENSP00000345728.6:n.1708-260_1708-259del
ENST00000343533.9:c.1708-260_1708-259del (ATP7A) ENSP00000343026.5:n.1708-260_1708-259del
ENST00000350425.5:c.*881-260_*881-259del (ATP7A) ENSP00000343678.5:n.*881-260_*881-259del
NM_000052.6:c.1708-260_1708-259del (ATP7A) NP_000043.4:n.1708-260_1708-259del
NM_001282224.1:c.1708-260_1708-259del (ATP7A) NP_001269153.1:n.1708-260_1708-259del
NR_104109.1:n.322-22558_322-22557del (ATP7A)
NM_000052.7:c.1708-260_1708-259del (ATP7A) MANE Select NP_000043.4:n.1708-260_1708-259del
NR_104109.2:n.285-22558_285-22557del (ATP7A)
NM_001282224.2:c.1708-260_1708-259del (ATP7A) NP_001269153.1:n.1708-260_1708-259del