Canonical Allele Identifier: CA421355510

Gene: COPA NHLH1

Linked Data

• MyVariant Identifiers: chr1:g.160283809C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160314019C>T , CM000663.2:g.160314019C>T	GRCh38
NC_000001.10:g.160283809C>T , CM000663.1:g.160283809C>T	GRCh37
NC_000001.9:g.158550433C>T	NCBI36
NG_050927.1:g.34546G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696202.1:n.485G>A (COPA)
ENST00000696203.1:n.3297G>A (COPA)
ENST00000696204.1:n.3504G>A (COPA)
ENST00000696206.1:n.584G>A (COPA)
ENST00000696207.1:n.810G>A (COPA)
ENST00000696208.1:n.916G>A (COPA)
ENST00000696209.1:n.1209G>A (COPA)
ENST00000696210.1:n.1209G>A (COPA)
ENST00000696211.1:n.1209G>A (COPA)
ENST00000696212.1:n.3497G>A (COPA)
ENST00000696213.1:n.1940G>A (COPA)
ENST00000696214.1:n.3523G>A (COPA)
ENST00000696215.1:n.916G>A (COPA)
ENST00000241704.8:c.813G>A (COPA) MANE Select	ENSP00000241704.7:p.Lys271=
ENST00000647683.1:c.813G>A (COPA)	ENSP00000497495.1:p.Lys271=
ENST00000647693.1:n.1897G>A (COPA)
ENST00000647799.1:c.*250G>A (COPA)	ENSP00000497970.1:n.*250G>A
ENST00000647899.1:c.332G>A (COPA)
ENST00000648501.1:c.316-852G>A (COPA)
ENST00000648805.1:c.813G>A (COPA)	ENSP00000497433.1:p.Lys271=
ENST00000649231.1:c.813G>A (COPA)	ENSP00000498061.1:p.Lys271=
ENST00000649676.1:c.360G>A (COPA)	ENSP00000497257.1:p.Lys120=
ENST00000649787.1:c.813G>A (COPA)	ENSP00000497231.1:p.Lys271=
ENST00000649963.1:c.*502G>A (COPA)	ENSP00000498129.1:n.*502G>A
ENST00000650154.1:c.*250G>A (COPA)	ENSP00000497094.1:n.*250G>A
ENST00000241704.7:c.813G>A (COPA)	ENSP00000241704.7:p.Lys271=
ENST00000368069.7:c.813G>A (COPA)	ENSP00000357048.3:p.Lys271=
NM_001098398.1:c.813G>A (COPA)	NP_001091868.1:p.Lys271=
NM_004371.3:c.813G>A (COPA)	NP_004362.2:p.Lys271=
XM_011509584.1:c.-176+27428C>T (NHLH1)	XP_011507886.1:n.-176+27428C>T
NM_001098398.2:c.813G>A (COPA)	NP_001091868.1:p.Lys271=
NM_004371.4:c.813G>A (COPA) MANE Select	NP_004362.2:p.Lys271=