Canonical Allele Identifier: CA343264166

Gene: COPA NHLH1

Linked Data

• MyVariant Identifiers: chr1:g.160283853A>C (hg19) ; chr1:g.160314063A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160314063A>C , CM000663.2:g.160314063A>C	GRCh38
NC_000001.10:g.160283853A>C , CM000663.1:g.160283853A>C	GRCh37
NC_000001.9:g.158550477A>C	NCBI36
NG_050927.1:g.34502T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696202.1:n.441T>G (COPA)
ENST00000696203.1:n.3253T>G (COPA)
ENST00000696204.1:n.3460T>G (COPA)
ENST00000696206.1:n.540T>G (COPA)
ENST00000696207.1:n.766T>G (COPA)
ENST00000696208.1:n.872T>G (COPA)
ENST00000696209.1:n.1165T>G (COPA)
ENST00000696210.1:n.1165T>G (COPA)
ENST00000696211.1:n.1165T>G (COPA)
ENST00000696212.1:n.3453T>G (COPA)
ENST00000696213.1:n.1896T>G (COPA)
ENST00000696214.1:n.3479T>G (COPA)
ENST00000696215.1:n.872T>G (COPA)
ENST00000241704.8:c.769T>G (COPA) MANE Select	ENSP00000241704.7:p.Phe257Val
ENST00000647683.1:c.769T>G (COPA)	ENSP00000497495.1:p.Phe257Val
ENST00000647693.1:n.1853T>G (COPA)
ENST00000647799.1:c.*206T>G (COPA)	ENSP00000497970.1:n.*206T>G
ENST00000647899.1:c.288T>G (COPA)
ENST00000648501.1:c.316-896T>G (COPA)
ENST00000648805.1:c.769T>G (COPA)	ENSP00000497433.1:p.Phe257Val
ENST00000649231.1:c.769T>G (COPA)	ENSP00000498061.1:p.Phe257Val
ENST00000649676.1:c.316T>G (COPA)	ENSP00000497257.1:p.Phe106Val
ENST00000649787.1:c.769T>G (COPA)	ENSP00000497231.1:p.Phe257Val
ENST00000649963.1:c.*458T>G (COPA)	ENSP00000498129.1:n.*458T>G
ENST00000650154.1:c.*206T>G (COPA)	ENSP00000497094.1:n.*206T>G
ENST00000241704.7:c.769T>G (COPA)	ENSP00000241704.7:p.Phe257Val
ENST00000368069.7:c.769T>G (COPA)	ENSP00000357048.3:p.Phe257Val
NM_001098398.1:c.769T>G (COPA)	NP_001091868.1:p.Phe257Val
NM_004371.3:c.769T>G (COPA)	NP_004362.2:p.Phe257Val
XM_011509584.1:c.-176+27472A>C (NHLH1)	XP_011507886.1:n.-176+27472A>C
NM_001098398.2:c.769T>G (COPA)	NP_001091868.1:p.Phe257Val
NM_004371.4:c.769T>G (COPA) MANE Select	NP_004362.2:p.Phe257Val