Canonical Allele Identifier: CA10459349

Linked Data

dbSNP Id: rs200420985
gnomAD v2: X-77276597-C-T
gnomAD v3: X-78021100-C-T
gnomAD v4: X-78021100-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.78021100C>T , CM000685.2:g.78021100C>T GRCh38
NC_000023.10:g.77276597C>T , CM000685.1:g.77276597C>T GRCh37
NC_000023.9:g.77163253C>T NCBI36
NG_013224.2:g.115404C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000343533.10:c.2946+21C>T (ATP7A) ENSP00000343026.6:n.2946+21C>T
ENST00000682475.1:n.1333+21C>T (ATP7A)
ENST00000685033.1:c.375+702C>T (ATP7A) ENSP00000509269.1:n.375+702C>T
ENST00000685264.1:c.2916+21C>T (ATP7A) ENSP00000510136.1:n.2916+21C>T
ENST00000686033.1:c.2916+21C>T (ATP7A) ENSP00000510693.1:n.2916+21C>T
ENST00000686133.1:c.2916+21C>T (ATP7A) ENSP00000509233.1:n.2916+21C>T
ENST00000686255.1:n.1947+21C>T (ATP7A)
ENST00000686543.1:c.2682+21C>T (ATP7A) ENSP00000509477.1:n.2682+21C>T
ENST00000687086.1:c.2916+21C>T (ATP7A) ENSP00000509566.1:n.2916+21C>T
ENST00000689514.1:n.958+21C>T (ATP7A)
ENST00000689767.1:c.3009+21C>T (ATP7A) ENSP00000509406.1:n.3009+21C>T
ENST00000692908.1:c.2682+21C>T (ATP7A) ENSP00000508627.1:n.2682+21C>T
ENST00000341514.11:c.2916+21C>T (ATP7A) MANE Select ENSP00000345728.6:n.2916+21C>T
ENST00000644362.1:c.-19-88767C>T (PGK1) ENSP00000496140.1:n.-19-88767C>T
ENST00000645094.1:c.*2830+21C>T (ATP7A) ENSP00000493605.1:n.*2830+21C>T
ENST00000341514.10:c.2916+21C>T (ATP7A) ENSP00000345728.6:n.2916+21C>T
ENST00000343533.9:c.2682+21C>T (ATP7A) ENSP00000343026.5:n.2682+21C>T
ENST00000350425.5:c.*2089+21C>T (ATP7A) ENSP00000343678.5:n.*2089+21C>T
NM_000052.6:c.2916+21C>T (ATP7A) NP_000043.4:n.2916+21C>T
NM_001282224.1:c.2682+21C>T (ATP7A) NP_001269153.1:n.2682+21C>T
NR_104109.1:n.322-10300C>T (ATP7A)
NM_000052.7:c.2916+21C>T (ATP7A) MANE Select NP_000043.4:n.2916+21C>T
NR_104109.2:n.285-10300C>T (ATP7A)
NM_001282224.2:c.2682+21C>T (ATP7A) NP_001269153.1:n.2682+21C>T