Canonical Allele Identifier: CA343263430

Gene: COPA NHLH1

Linked Data

• MyVariant Identifiers: chr1:g.160283783T>A (hg19) ; chr1:g.160313993T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160313993T>A , CM000663.2:g.160313993T>A	GRCh38
NC_000001.10:g.160283783T>A , CM000663.1:g.160283783T>A	GRCh37
NC_000001.9:g.158550407T>A	NCBI36
NG_050927.1:g.34572A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696202.1:n.511A>T (COPA)
ENST00000696203.1:n.3323A>T (COPA)
ENST00000696204.1:n.3530A>T (COPA)
ENST00000696206.1:n.610A>T (COPA)
ENST00000696207.1:n.836A>T (COPA)
ENST00000696208.1:n.942A>T (COPA)
ENST00000696209.1:n.1235A>T (COPA)
ENST00000696210.1:n.1235A>T (COPA)
ENST00000696211.1:n.1235A>T (COPA)
ENST00000696212.1:n.3523A>T (COPA)
ENST00000696213.1:n.1966A>T (COPA)
ENST00000696214.1:n.3549A>T (COPA)
ENST00000696215.1:n.942A>T (COPA)
ENST00000241704.8:c.839A>T (COPA) MANE Select	ENSP00000241704.7:p.Lys280Met
ENST00000647683.1:c.839A>T (COPA)	ENSP00000497495.1:p.Lys280Met
ENST00000647693.1:n.1923A>T (COPA)
ENST00000647799.1:c.*276A>T (COPA)	ENSP00000497970.1:n.*276A>T
ENST00000647899.1:c.358A>T (COPA)
ENST00000648501.1:c.316-826A>T (COPA)
ENST00000648805.1:c.839A>T (COPA)	ENSP00000497433.1:p.Lys280Met
ENST00000649231.1:c.839A>T (COPA)	ENSP00000498061.1:p.Lys280Met
ENST00000649676.1:c.386A>T (COPA)	ENSP00000497257.1:p.Lys129Met
ENST00000649787.1:c.839A>T (COPA)	ENSP00000497231.1:p.Lys280Met
ENST00000649963.1:c.*528A>T (COPA)	ENSP00000498129.1:n.*528A>T
ENST00000650154.1:c.*276A>T (COPA)	ENSP00000497094.1:n.*276A>T
ENST00000241704.7:c.839A>T (COPA)	ENSP00000241704.7:p.Lys280Met
ENST00000368069.7:c.839A>T (COPA)	ENSP00000357048.3:p.Lys280Met
NM_001098398.1:c.839A>T (COPA)	NP_001091868.1:p.Lys280Met
NM_004371.3:c.839A>T (COPA)	NP_004362.2:p.Lys280Met
XM_011509584.1:c.-176+27402T>A (NHLH1)	XP_011507886.1:n.-176+27402T>A
NM_001098398.2:c.839A>T (COPA)	NP_001091868.1:p.Lys280Met
NM_004371.4:c.839A>T (COPA) MANE Select	NP_004362.2:p.Lys280Met