Canonical Allele Identifier: CA331105997

Linked Data

dbSNP Id: rs989216537
gnomAD v2: X-77289007-T-C
gnomAD v3: X-78033509-T-C
gnomAD v4: X-78033509-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.78033509T>C , CM000685.2:g.78033509T>C GRCh38
NC_000023.10:g.77289007T>C , CM000685.1:g.77289007T>C GRCh37
NC_000023.9:g.77175663T>C NCBI36
NG_013224.2:g.127813T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000343533.10:c.3325-96T>C (ATP7A) ENSP00000343026.6:n.3325-96T>C
ENST00000682475.1:n.1712-96T>C (ATP7A)
ENST00000685033.1:c.559-96T>C (ATP7A) ENSP00000509269.1:n.559-96T>C
ENST00000685264.1:c.3295-96T>C (ATP7A) ENSP00000510136.1:n.3295-96T>C
ENST00000686033.1:c.3100-96T>C (ATP7A) ENSP00000510693.1:n.3100-96T>C
ENST00000686133.1:c.3295-96T>C (ATP7A) ENSP00000509233.1:n.3295-96T>C
ENST00000686255.1:n.2326-96T>C (ATP7A)
ENST00000686543.1:c.3061-96T>C (ATP7A) ENSP00000509477.1:n.3061-96T>C
ENST00000687086.1:c.3295-96T>C (ATP7A) ENSP00000509566.1:n.3295-96T>C
ENST00000689514.1:n.1337-96T>C (ATP7A)
ENST00000689767.1:c.3388-96T>C (ATP7A) ENSP00000509406.1:n.3388-96T>C
ENST00000692908.1:c.3061-96T>C (ATP7A) ENSP00000508627.1:n.3061-96T>C
ENST00000341514.11:c.3295-96T>C (ATP7A) MANE Select ENSP00000345728.6:n.3295-96T>C
ENST00000644362.1:c.-19-76358T>C (PGK1) ENSP00000496140.1:n.-19-76358T>C
ENST00000645094.1:c.*3209-96T>C (ATP7A) ENSP00000493605.1:n.*3209-96T>C
ENST00000341514.10:c.3295-96T>C (ATP7A) ENSP00000345728.6:n.3295-96T>C
ENST00000343533.9:c.3061-96T>C (ATP7A) ENSP00000343026.5:n.3061-96T>C
ENST00000350425.5:c.*2468-96T>C (ATP7A) ENSP00000343678.5:n.*2468-96T>C
NM_000052.6:c.3295-96T>C (ATP7A) NP_000043.4:n.3295-96T>C
NM_001282224.1:c.3061-96T>C (ATP7A) NP_001269153.1:n.3061-96T>C
NR_104109.1:n.505-96T>C (ATP7A)
NM_000052.7:c.3295-96T>C (ATP7A) MANE Select NP_000043.4:n.3295-96T>C
NR_104109.2:n.468-96T>C (ATP7A)
NM_001282224.2:c.3061-96T>C (ATP7A) NP_001269153.1:n.3061-96T>C