Canonical Allele Identifier: CA277215

Linked Data

ClinVar Variation Id: 210400
ClinVar RCV Id: RCV000193862
dbSNP Id: rs797045337

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.78009225G>T , CM000685.2:g.78009225G>T GRCh38
NC_000023.10:g.77264722G>T , CM000685.1:g.77264722G>T GRCh37
NC_000023.9:g.77151378G>T NCBI36
NG_013224.2:g.103529G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000343533.10:c.1861G>T (ATP7A) ENSP00000343026.6:p.Glu621Ter
ENST00000682742.2:n.1993G>T (ATP7A)
ENST00000685264.1:c.1831G>T (ATP7A) ENSP00000510136.1:p.Glu611Ter
ENST00000685434.1:n.1865G>T (ATP7A)
ENST00000686033.1:c.1831G>T (ATP7A) ENSP00000510693.1:p.Glu611Ter
ENST00000686133.1:c.1831G>T (ATP7A) ENSP00000509233.1:p.Glu611Ter
ENST00000686416.1:n.2185G>T (ATP7A)
ENST00000686480.1:c.1831G>T (ATP7A) ENSP00000508978.1:p.Glu611Ter
ENST00000686515.1:n.1971G>T (ATP7A)
ENST00000686543.1:c.1831G>T (ATP7A) ENSP00000509477.1:p.Glu611Ter
ENST00000686688.1:c.1831G>T (ATP7A) ENSP00000509416.1:p.Glu611Ter
ENST00000686999.1:n.2142G>T (ATP7A)
ENST00000687086.1:c.1831G>T (ATP7A) ENSP00000509566.1:p.Glu611Ter
ENST00000687628.1:n.1932G>T (ATP7A)
ENST00000688746.1:n.1983G>T (ATP7A)
ENST00000689530.1:c.1831G>T (ATP7A) ENSP00000509707.1:p.Glu611Ter
ENST00000689541.1:n.2140G>T (ATP7A)
ENST00000689649.1:c.1831G>T (ATP7A) ENSP00000509277.1:p.Glu611Ter
ENST00000689767.1:c.1924G>T (ATP7A) ENSP00000509406.1:p.Glu642Ter
ENST00000689872.1:c.1831G>T (ATP7A) ENSP00000509373.1:p.Glu611Ter
ENST00000692110.1:c.1747G>T (ATP7A) ENSP00000509366.1:p.Glu583Ter
ENST00000692908.1:c.1831G>T (ATP7A) ENSP00000508627.1:p.Glu611Ter
ENST00000693387.1:c.*1760G>T (ATP7A) ENSP00000508732.1:n.*1760G>T
ENST00000693398.1:c.1831G>T (ATP7A) ENSP00000510089.1:p.Glu611Ter
ENST00000341514.11:c.1831G>T (ATP7A) MANE Select ENSP00000345728.6:p.Glu611Ter
ENST00000644362.1:c.-20+98390G>T (PGK1) ENSP00000496140.1:n.-20+98390G>T
ENST00000645094.1:c.*1745G>T (ATP7A) ENSP00000493605.1:n.*1745G>T
ENST00000341514.10:c.1831G>T (ATP7A) ENSP00000345728.6:p.Glu611Ter
ENST00000343533.9:c.1831G>T (ATP7A) ENSP00000343026.5:p.Glu611Ter
ENST00000350425.5:c.*1004G>T (ATP7A) ENSP00000343678.5:n.*1004G>T
NM_000052.6:c.1831G>T (ATP7A) NP_000043.4:p.Glu611Ter
NM_001282224.1:c.1831G>T (ATP7A) NP_001269153.1:p.Glu611Ter
NR_104109.1:n.322-22175G>T (ATP7A)
NM_000052.7:c.1831G>T (ATP7A) MANE Select NP_000043.4:p.Glu611Ter
NR_104109.2:n.285-22175G>T (ATP7A)
NM_001282224.2:c.1831G>T (ATP7A) NP_001269153.1:p.Glu611Ter