Canonical Allele Identifier: CA421355413

Linked Data

MyVariant Identifiers: chr1:g.160283791A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160314001A>G , CM000663.2:g.160314001A>G GRCh38
NC_000001.10:g.160283791A>G , CM000663.1:g.160283791A>G GRCh37
NC_000001.9:g.158550415A>G NCBI36
NG_050927.1:g.34564T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000696202.1:n.503T>C (COPA)
ENST00000696203.1:n.3315T>C (COPA)
ENST00000696204.1:n.3522T>C (COPA)
ENST00000696206.1:n.602T>C (COPA)
ENST00000696207.1:n.828T>C (COPA)
ENST00000696208.1:n.934T>C (COPA)
ENST00000696209.1:n.1227T>C (COPA)
ENST00000696210.1:n.1227T>C (COPA)
ENST00000696211.1:n.1227T>C (COPA)
ENST00000696212.1:n.3515T>C (COPA)
ENST00000696213.1:n.1958T>C (COPA)
ENST00000696214.1:n.3541T>C (COPA)
ENST00000696215.1:n.934T>C (COPA)
ENST00000241704.8:c.831T>C (COPA) MANE Select ENSP00000241704.7:p.Asp277=
ENST00000647683.1:c.831T>C (COPA) ENSP00000497495.1:p.Asp277=
ENST00000647693.1:n.1915T>C (COPA)
ENST00000647799.1:c.*268T>C (COPA) ENSP00000497970.1:n.*268T>C
ENST00000647899.1:c.350T>C (COPA)
ENST00000648501.1:c.316-834T>C (COPA)
ENST00000648805.1:c.831T>C (COPA) ENSP00000497433.1:p.Asp277=
ENST00000649231.1:c.831T>C (COPA) ENSP00000498061.1:p.Asp277=
ENST00000649676.1:c.378T>C (COPA) ENSP00000497257.1:p.Asp126=
ENST00000649787.1:c.831T>C (COPA) ENSP00000497231.1:p.Asp277=
ENST00000649963.1:c.*520T>C (COPA) ENSP00000498129.1:n.*520T>C
ENST00000650154.1:c.*268T>C (COPA) ENSP00000497094.1:n.*268T>C
ENST00000241704.7:c.831T>C (COPA) ENSP00000241704.7:p.Asp277=
ENST00000368069.7:c.831T>C (COPA) ENSP00000357048.3:p.Asp277=
NM_001098398.1:c.831T>C (COPA) NP_001091868.1:p.Asp277=
NM_004371.3:c.831T>C (COPA) NP_004362.2:p.Asp277=
XM_011509584.1:c.-176+27410A>G (NHLH1) XP_011507886.1:n.-176+27410A>G
NM_001098398.2:c.831T>C (COPA) NP_001091868.1:p.Asp277=
NM_004371.4:c.831T>C (COPA) MANE Select NP_004362.2:p.Asp277=