Canonical Allele Identifier: CA343264163

Gene: COPA NHLH1

Linked Data

• MyVariant Identifiers: chr1:g.160283852A>T (hg19) ; chr1:g.160314062A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160314062A>T , CM000663.2:g.160314062A>T	GRCh38
NC_000001.10:g.160283852A>T , CM000663.1:g.160283852A>T	GRCh37
NC_000001.9:g.158550476A>T	NCBI36
NG_050927.1:g.34503T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696202.1:n.442T>A (COPA)
ENST00000696203.1:n.3254T>A (COPA)
ENST00000696204.1:n.3461T>A (COPA)
ENST00000696206.1:n.541T>A (COPA)
ENST00000696207.1:n.767T>A (COPA)
ENST00000696208.1:n.873T>A (COPA)
ENST00000696209.1:n.1166T>A (COPA)
ENST00000696210.1:n.1166T>A (COPA)
ENST00000696211.1:n.1166T>A (COPA)
ENST00000696212.1:n.3454T>A (COPA)
ENST00000696213.1:n.1897T>A (COPA)
ENST00000696214.1:n.3480T>A (COPA)
ENST00000696215.1:n.873T>A (COPA)
ENST00000241704.8:c.770T>A (COPA) MANE Select	ENSP00000241704.7:p.Phe257Tyr
ENST00000647683.1:c.770T>A (COPA)	ENSP00000497495.1:p.Phe257Tyr
ENST00000647693.1:n.1854T>A (COPA)
ENST00000647799.1:c.*207T>A (COPA)	ENSP00000497970.1:n.*207T>A
ENST00000647899.1:c.289T>A (COPA)
ENST00000648501.1:c.316-895T>A (COPA)
ENST00000648805.1:c.770T>A (COPA)	ENSP00000497433.1:p.Phe257Tyr
ENST00000649231.1:c.770T>A (COPA)	ENSP00000498061.1:p.Phe257Tyr
ENST00000649676.1:c.317T>A (COPA)	ENSP00000497257.1:p.Phe106Tyr
ENST00000649787.1:c.770T>A (COPA)	ENSP00000497231.1:p.Phe257Tyr
ENST00000649963.1:c.*459T>A (COPA)	ENSP00000498129.1:n.*459T>A
ENST00000650154.1:c.*207T>A (COPA)	ENSP00000497094.1:n.*207T>A
ENST00000241704.7:c.770T>A (COPA)	ENSP00000241704.7:p.Phe257Tyr
ENST00000368069.7:c.770T>A (COPA)	ENSP00000357048.3:p.Phe257Tyr
NM_001098398.1:c.770T>A (COPA)	NP_001091868.1:p.Phe257Tyr
NM_004371.3:c.770T>A (COPA)	NP_004362.2:p.Phe257Tyr
XM_011509584.1:c.-176+27471A>T (NHLH1)	XP_011507886.1:n.-176+27471A>T
NM_001098398.2:c.770T>A (COPA)	NP_001091868.1:p.Phe257Tyr
NM_004371.4:c.770T>A (COPA) MANE Select	NP_004362.2:p.Phe257Tyr