Canonical Allele Identifier: CA343264472

Gene: COPA NHLH1

Linked Data

• MyVariant Identifiers: chr1:g.160283894T>A (hg19) ; chr1:g.160314104T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160314104T>A , CM000663.2:g.160314104T>A	GRCh38
NC_000001.10:g.160283894T>A , CM000663.1:g.160283894T>A	GRCh37
NC_000001.9:g.158550518T>A	NCBI36
NG_050927.1:g.34461A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696202.1:n.400A>T (COPA)
ENST00000696203.1:n.3212A>T (COPA)
ENST00000696204.1:n.3419A>T (COPA)
ENST00000696206.1:n.499A>T (COPA)
ENST00000696207.1:n.725A>T (COPA)
ENST00000696208.1:n.831A>T (COPA)
ENST00000696209.1:n.1124A>T (COPA)
ENST00000696210.1:n.1124A>T (COPA)
ENST00000696211.1:n.1124A>T (COPA)
ENST00000696212.1:n.3412A>T (COPA)
ENST00000696213.1:n.1855A>T (COPA)
ENST00000696214.1:n.3438A>T (COPA)
ENST00000696215.1:n.831A>T (COPA)
ENST00000241704.8:c.728A>T (COPA) MANE Select	ENSP00000241704.7:p.Asp243Val
ENST00000647683.1:c.728A>T (COPA)	ENSP00000497495.1:p.Asp243Val
ENST00000647693.1:n.1812A>T (COPA)
ENST00000647799.1:c.*165A>T (COPA)	ENSP00000497970.1:n.*165A>T
ENST00000647899.1:c.247A>T (COPA)
ENST00000648501.1:c.316-937A>T (COPA)
ENST00000648805.1:c.728A>T (COPA)	ENSP00000497433.1:p.Asp243Val
ENST00000649231.1:c.728A>T (COPA)	ENSP00000498061.1:p.Asp243Val
ENST00000649676.1:c.275A>T (COPA)	ENSP00000497257.1:p.Asp92Val
ENST00000649787.1:c.728A>T (COPA)	ENSP00000497231.1:p.Asp243Val
ENST00000649963.1:c.*417A>T (COPA)	ENSP00000498129.1:n.*417A>T
ENST00000650154.1:c.*165A>T (COPA)	ENSP00000497094.1:n.*165A>T
ENST00000241704.7:c.728A>T (COPA)	ENSP00000241704.7:p.Asp243Val
ENST00000368069.7:c.728A>T (COPA)	ENSP00000357048.3:p.Asp243Val
NM_001098398.1:c.728A>T (COPA)	NP_001091868.1:p.Asp243Val
NM_004371.3:c.728A>T (COPA)	NP_004362.2:p.Asp243Val
XM_011509584.1:c.-176+27513T>A (NHLH1)	XP_011507886.1:n.-176+27513T>A
NM_001098398.2:c.728A>T (COPA)	NP_001091868.1:p.Asp243Val
NM_004371.4:c.728A>T (COPA) MANE Select	NP_004362.2:p.Asp243Val