Canonical Allele Identifier: CA343263630

Gene: COPA NHLH1

Linked Data

• MyVariant Identifiers: chr1:g.160283793C>A (hg19) ; chr1:g.160314003C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160314003C>A , CM000663.2:g.160314003C>A	GRCh38
NC_000001.10:g.160283793C>A , CM000663.1:g.160283793C>A	GRCh37
NC_000001.9:g.158550417C>A	NCBI36
NG_050927.1:g.34562G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696202.1:n.501G>T (COPA)
ENST00000696203.1:n.3313G>T (COPA)
ENST00000696204.1:n.3520G>T (COPA)
ENST00000696206.1:n.600G>T (COPA)
ENST00000696207.1:n.826G>T (COPA)
ENST00000696208.1:n.932G>T (COPA)
ENST00000696209.1:n.1225G>T (COPA)
ENST00000696210.1:n.1225G>T (COPA)
ENST00000696211.1:n.1225G>T (COPA)
ENST00000696212.1:n.3513G>T (COPA)
ENST00000696213.1:n.1956G>T (COPA)
ENST00000696214.1:n.3539G>T (COPA)
ENST00000696215.1:n.932G>T (COPA)
ENST00000241704.8:c.829G>T (COPA) MANE Select	ENSP00000241704.7:p.Asp277Tyr
ENST00000647683.1:c.829G>T (COPA)	ENSP00000497495.1:p.Asp277Tyr
ENST00000647693.1:n.1913G>T (COPA)
ENST00000647799.1:c.*266G>T (COPA)	ENSP00000497970.1:n.*266G>T
ENST00000647899.1:c.348G>T (COPA)
ENST00000648501.1:c.316-836G>T (COPA)
ENST00000648805.1:c.829G>T (COPA)	ENSP00000497433.1:p.Asp277Tyr
ENST00000649231.1:c.829G>T (COPA)	ENSP00000498061.1:p.Asp277Tyr
ENST00000649676.1:c.376G>T (COPA)	ENSP00000497257.1:p.Asp126Tyr
ENST00000649787.1:c.829G>T (COPA)	ENSP00000497231.1:p.Asp277Tyr
ENST00000649963.1:c.*518G>T (COPA)	ENSP00000498129.1:n.*518G>T
ENST00000650154.1:c.*266G>T (COPA)	ENSP00000497094.1:n.*266G>T
ENST00000241704.7:c.829G>T (COPA)	ENSP00000241704.7:p.Asp277Tyr
ENST00000368069.7:c.829G>T (COPA)	ENSP00000357048.3:p.Asp277Tyr
NM_001098398.1:c.829G>T (COPA)	NP_001091868.1:p.Asp277Tyr
NM_004371.3:c.829G>T (COPA)	NP_004362.2:p.Asp277Tyr
XM_011509584.1:c.-176+27412C>A (NHLH1)	XP_011507886.1:n.-176+27412C>A
NM_001098398.2:c.829G>T (COPA)	NP_001091868.1:p.Asp277Tyr
NM_004371.4:c.829G>T (COPA) MANE Select	NP_004362.2:p.Asp277Tyr