Canonical Allele Identifier: CA343264305

Gene: COPA NHLH1

Linked Data

• MyVariant Identifiers: chr1:g.160283869A>T (hg19) ; chr1:g.160314079A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160314079A>T , CM000663.2:g.160314079A>T	GRCh38
NC_000001.10:g.160283869A>T , CM000663.1:g.160283869A>T	GRCh37
NC_000001.9:g.158550493A>T	NCBI36
NG_050927.1:g.34486T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696202.1:n.425T>A (COPA)
ENST00000696203.1:n.3237T>A (COPA)
ENST00000696204.1:n.3444T>A (COPA)
ENST00000696206.1:n.524T>A (COPA)
ENST00000696207.1:n.750T>A (COPA)
ENST00000696208.1:n.856T>A (COPA)
ENST00000696209.1:n.1149T>A (COPA)
ENST00000696210.1:n.1149T>A (COPA)
ENST00000696211.1:n.1149T>A (COPA)
ENST00000696212.1:n.3437T>A (COPA)
ENST00000696213.1:n.1880T>A (COPA)
ENST00000696214.1:n.3463T>A (COPA)
ENST00000696215.1:n.856T>A (COPA)
ENST00000241704.8:c.753T>A (COPA) MANE Select	ENSP00000241704.7:p.Asn251Lys
ENST00000647683.1:c.753T>A (COPA)	ENSP00000497495.1:p.Asn251Lys
ENST00000647693.1:n.1837T>A (COPA)
ENST00000647799.1:c.*190T>A (COPA)	ENSP00000497970.1:n.*190T>A
ENST00000647899.1:c.272T>A (COPA)
ENST00000648501.1:c.316-912T>A (COPA)
ENST00000648805.1:c.753T>A (COPA)	ENSP00000497433.1:p.Asn251Lys
ENST00000649231.1:c.753T>A (COPA)	ENSP00000498061.1:p.Asn251Lys
ENST00000649676.1:c.300T>A (COPA)	ENSP00000497257.1:p.Asn100Lys
ENST00000649787.1:c.753T>A (COPA)	ENSP00000497231.1:p.Asn251Lys
ENST00000649963.1:c.*442T>A (COPA)	ENSP00000498129.1:n.*442T>A
ENST00000650154.1:c.*190T>A (COPA)	ENSP00000497094.1:n.*190T>A
ENST00000241704.7:c.753T>A (COPA)	ENSP00000241704.7:p.Asn251Lys
ENST00000368069.7:c.753T>A (COPA)	ENSP00000357048.3:p.Asn251Lys
NM_001098398.1:c.753T>A (COPA)	NP_001091868.1:p.Asn251Lys
NM_004371.3:c.753T>A (COPA)	NP_004362.2:p.Asn251Lys
XM_011509584.1:c.-176+27488A>T (NHLH1)	XP_011507886.1:n.-176+27488A>T
NM_001098398.2:c.753T>A (COPA)	NP_001091868.1:p.Asn251Lys
NM_004371.4:c.753T>A (COPA) MANE Select	NP_004362.2:p.Asn251Lys