Canonical Allele Identifier: CA343263651

Gene: COPA NHLH1

Linked Data

• MyVariant Identifiers: chr1:g.160283796A>G (hg19) ; chr1:g.160314006A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160314006A>G , CM000663.2:g.160314006A>G	GRCh38
NC_000001.10:g.160283796A>G , CM000663.1:g.160283796A>G	GRCh37
NC_000001.9:g.158550420A>G	NCBI36
NG_050927.1:g.34559T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696202.1:n.498T>C (COPA)
ENST00000696203.1:n.3310T>C (COPA)
ENST00000696204.1:n.3517T>C (COPA)
ENST00000696206.1:n.597T>C (COPA)
ENST00000696207.1:n.823T>C (COPA)
ENST00000696208.1:n.929T>C (COPA)
ENST00000696209.1:n.1222T>C (COPA)
ENST00000696210.1:n.1222T>C (COPA)
ENST00000696211.1:n.1222T>C (COPA)
ENST00000696212.1:n.3510T>C (COPA)
ENST00000696213.1:n.1953T>C (COPA)
ENST00000696214.1:n.3536T>C (COPA)
ENST00000696215.1:n.929T>C (COPA)
ENST00000241704.8:c.826T>C (COPA) MANE Select	ENSP00000241704.7:p.Trp276Arg
ENST00000647683.1:c.826T>C (COPA)	ENSP00000497495.1:p.Trp276Arg
ENST00000647693.1:n.1910T>C (COPA)
ENST00000647799.1:c.*263T>C (COPA)	ENSP00000497970.1:n.*263T>C
ENST00000647899.1:c.345T>C (COPA)
ENST00000648501.1:c.316-839T>C (COPA)
ENST00000648805.1:c.826T>C (COPA)	ENSP00000497433.1:p.Trp276Arg
ENST00000649231.1:c.826T>C (COPA)	ENSP00000498061.1:p.Trp276Arg
ENST00000649676.1:c.373T>C (COPA)	ENSP00000497257.1:p.Trp125Arg
ENST00000649787.1:c.826T>C (COPA)	ENSP00000497231.1:p.Trp276Arg
ENST00000649963.1:c.*515T>C (COPA)	ENSP00000498129.1:n.*515T>C
ENST00000650154.1:c.*263T>C (COPA)	ENSP00000497094.1:n.*263T>C
ENST00000241704.7:c.826T>C (COPA)	ENSP00000241704.7:p.Trp276Arg
ENST00000368069.7:c.826T>C (COPA)	ENSP00000357048.3:p.Trp276Arg
NM_001098398.1:c.826T>C (COPA)	NP_001091868.1:p.Trp276Arg
NM_004371.3:c.826T>C (COPA)	NP_004362.2:p.Trp276Arg
XM_011509584.1:c.-176+27415A>G (NHLH1)	XP_011507886.1:n.-176+27415A>G
NM_001098398.2:c.826T>C (COPA)	NP_001091868.1:p.Trp276Arg
NM_004371.4:c.826T>C (COPA) MANE Select	NP_004362.2:p.Trp276Arg