Canonical Allele Identifier: CA2573939200

Gene: COPA NHLH1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160313893A>T , CM000663.2:g.160313893A>T	GRCh38
NC_000001.10:g.160283683A>T , CM000663.1:g.160283683A>T	GRCh37
NC_000001.9:g.158550307A>T	NCBI36
NG_050927.1:g.34672T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696202.1:n.514+97T>A (COPA)
ENST00000696203.1:n.3326+97T>A (COPA)
ENST00000696204.1:n.3533+97T>A (COPA)
ENST00000696206.1:n.613+97T>A (COPA)
ENST00000696207.1:n.839+97T>A (COPA)
ENST00000696208.1:n.945+97T>A (COPA)
ENST00000696209.1:n.1238+97T>A (COPA)
ENST00000696210.1:n.1238+97T>A (COPA)
ENST00000696211.1:n.1238+97T>A (COPA)
ENST00000696212.1:n.3526+97T>A (COPA)
ENST00000696213.1:n.1969+97T>A (COPA)
ENST00000696214.1:n.3552+97T>A (COPA)
ENST00000696215.1:n.945+97T>A (COPA)
ENST00000241704.8:c.842+97T>A (COPA) MANE Select	ENSP00000241704.7:n.842+97T>A
ENST00000647683.1:c.842+97T>A (COPA)	ENSP00000497495.1:n.842+97T>A
ENST00000647693.1:n.1926+97T>A (COPA)
ENST00000647799.1:c.*279+97T>A (COPA)	ENSP00000497970.1:n.*279+97T>A
ENST00000647899.1:c.361+97T>A (COPA)
ENST00000648501.1:c.316-726T>A (COPA)
ENST00000648805.1:c.842+97T>A (COPA)	ENSP00000497433.1:n.842+97T>A
ENST00000649231.1:c.842+97T>A (COPA)	ENSP00000498061.1:n.842+97T>A
ENST00000649676.1:c.389+97T>A (COPA)	ENSP00000497257.1:n.389+97T>A
ENST00000649787.1:c.842+97T>A (COPA)	ENSP00000497231.1:n.842+97T>A
ENST00000649963.1:c.*531+97T>A (COPA)	ENSP00000498129.1:n.*531+97T>A
ENST00000650154.1:c.*279+97T>A (COPA)	ENSP00000497094.1:n.*279+97T>A
ENST00000241704.7:c.842+97T>A (COPA)	ENSP00000241704.7:n.842+97T>A
ENST00000368069.7:c.842+97T>A (COPA)	ENSP00000357048.3:n.842+97T>A
NM_001098398.1:c.842+97T>A (COPA)	NP_001091868.1:n.842+97T>A
NM_004371.3:c.842+97T>A (COPA)	NP_004362.2:n.842+97T>A
XM_011509584.1:c.-176+27302A>T (NHLH1)	XP_011507886.1:n.-176+27302A>T
NM_001098398.2:c.842+97T>A (COPA)	NP_001091868.1:n.842+97T>A
NM_004371.4:c.842+97T>A (COPA) MANE Select	NP_004362.2:n.842+97T>A