Canonical Allele Identifier: CA1202267857

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160314111C= , CM000663.2:g.160314111C= GRCh38
NC_000001.10:g.160283901C= , CM000663.1:g.160283901C= GRCh37
NC_000001.9:g.158550525C= NCBI36
NG_050927.1:g.34454G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696202.1:n.393G= (COPA)
ENST00000696203.1:n.3205G= (COPA)
ENST00000696204.1:n.3412G= (COPA)
ENST00000696206.1:n.492G= (COPA)
ENST00000696207.1:n.718G= (COPA)
ENST00000696208.1:n.824G= (COPA)
ENST00000696209.1:n.1117G= (COPA)
ENST00000696210.1:n.1117G= (COPA)
ENST00000696211.1:n.1117G= (COPA)
ENST00000696212.1:n.3405G= (COPA)
ENST00000696213.1:n.1848G= (COPA)
ENST00000696214.1:n.3431G= (COPA)
ENST00000696215.1:n.824G= (COPA)
ENST00000241704.8:c.721G= (COPA) MANE Select ENSP00000241704.7:p.Glu241=
ENST00000647683.1:c.721G= (COPA) ENSP00000497495.1:p.Glu241=
ENST00000647693.1:n.1805G= (COPA)
ENST00000647799.1:c.*158G= (COPA) ENSP00000497970.1:n.*158G=
ENST00000647899.1:c.240G= (COPA)
ENST00000648501.1:c.316-944G= (COPA)
ENST00000648805.1:c.721G= (COPA) ENSP00000497433.1:p.Glu241=
ENST00000649231.1:c.721G= (COPA) ENSP00000498061.1:p.Glu241=
ENST00000649676.1:c.268G= (COPA) ENSP00000497257.1:p.Glu90=
ENST00000649787.1:c.721G= (COPA) ENSP00000497231.1:p.Glu241=
ENST00000649963.1:c.*410G= (COPA) ENSP00000498129.1:n.*410G=
ENST00000650154.1:c.*158G= (COPA) ENSP00000497094.1:n.*158G=
ENST00000241704.7:c.721G= (COPA) ENSP00000241704.7:p.Glu241=
ENST00000368069.7:c.721G= (COPA) ENSP00000357048.3:p.Glu241=
NM_001098398.1:c.721G= (COPA) NP_001091868.1:p.Glu241=
NM_004371.3:c.721G= (COPA) NP_004362.2:p.Glu241=
XM_011509584.1:c.-176+27520C= (NHLH1) XP_011507886.1:n.-176+27520C=
NM_001098398.2:c.721G= (COPA) NP_001091868.1:p.Glu241=
NM_004371.4:c.721G= (COPA) MANE Select NP_004362.2:p.Glu241=