Canonical Allele Identifier: CA413604320

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.78033818T>C , CM000685.2:g.78033818T>C GRCh38
NC_000023.10:g.77289316T>C , CM000685.1:g.77289316T>C GRCh37
NC_000023.9:g.77175972T>C NCBI36
NG_013224.2:g.128122T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000343533.10:c.3538T>C (ATP7A) ENSP00000343026.6:p.Ser1180Pro
ENST00000682475.1:n.1925T>C (ATP7A)
ENST00000685033.1:c.772T>C (ATP7A) ENSP00000509269.1:p.Ser258Pro
ENST00000685264.1:c.3508T>C (ATP7A) ENSP00000510136.1:p.Ser1170Pro
ENST00000686033.1:c.3313T>C (ATP7A) ENSP00000510693.1:p.Ser1105Pro
ENST00000686133.1:c.3508T>C (ATP7A) ENSP00000509233.1:p.Ser1170Pro
ENST00000686255.1:n.2539T>C (ATP7A)
ENST00000686543.1:c.3274T>C (ATP7A) ENSP00000509477.1:p.Ser1092Pro
ENST00000687086.1:c.3508T>C (ATP7A) ENSP00000509566.1:p.Ser1170Pro
ENST00000689514.1:n.1550T>C (ATP7A)
ENST00000689767.1:c.3601T>C (ATP7A) ENSP00000509406.1:p.Ser1201Pro
ENST00000692908.1:c.3274T>C (ATP7A) ENSP00000508627.1:p.Ser1092Pro
ENST00000341514.11:c.3508T>C (ATP7A) MANE Select ENSP00000345728.6:p.Ser1170Pro
ENST00000644362.1:c.-19-76049T>C (PGK1) ENSP00000496140.1:n.-19-76049T>C
ENST00000645094.1:c.*3422T>C (ATP7A) ENSP00000493605.1:n.*3422T>C
ENST00000341514.10:c.3508T>C (ATP7A) ENSP00000345728.6:p.Ser1170Pro
ENST00000343533.9:c.3274T>C (ATP7A) ENSP00000343026.5:p.Ser1092Pro
ENST00000350425.5:c.*2681T>C (ATP7A) ENSP00000343678.5:n.*2681T>C
NM_000052.6:c.3508T>C (ATP7A) NP_000043.4:p.Ser1170Pro
NM_001282224.1:c.3274T>C (ATP7A) NP_001269153.1:p.Ser1092Pro
NR_104109.1:n.718T>C (ATP7A)
NM_000052.7:c.3508T>C (ATP7A) MANE Select NP_000043.4:p.Ser1170Pro
NR_104109.2:n.681T>C (ATP7A)
NM_001282224.2:c.3274T>C (ATP7A) NP_001269153.1:p.Ser1092Pro