Canonical Allele Identifier: CA2216454694

Gene: CORO1A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30186661G= , CM000678.2:g.30186661G=	GRCh38
NC_000016.9:g.30197982G= , CM000678.1:g.30197982G=	GRCh37
NC_000016.8:g.30105483G=	NCBI36
NG_023415.1:g.8057G= , LRG_195:g.8057G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696217.1:n.248G=
ENST00000219150.10:c.262G= MANE Select	ENSP00000219150.6:p.Ala88=
ENST00000219150.9:c.262G=	ENSP00000219150.5:p.Ala88=
ENST00000561815.5:c.370G=	ENSP00000456756.1:p.Ala124=
ENST00000563778.5:c.262G=	ENSP00000456266.1:p.Ala88=
ENST00000565497.5:c.262G=	ENSP00000456457.1:p.Ala88=
ENST00000567034.5:n.730G=
ENST00000568763.1:n.1574G=
ENST00000568982.5:n.380G=
ENST00000569203.5:c.262G=	ENSP00000454752.1:p.Ala88=
ENST00000569469.1:n.372G=
ENST00000569970.1:c.262G=	ENSP00000457509.1:p.Ala88=
ENST00000570045.5:c.262G=	ENSP00000455552.1:p.Ala88=
ENST00000570244.5:c.199-155G=	ENSP00000457332.1:n.199-155G=
NM_001193333.2:c.262G=	NP_001180262.1:p.Ala88=
NM_007074.3:c.262G=	NP_009005.1:p.Ala88=
XM_011545714.1:c.262G=	XP_011544016.1:p.Ala88=
XM_011545714.2:c.262G=	XP_011544016.1:p.Ala88=
XM_017022885.2:c.262G=	XP_016878374.1:p.Ala88=
XM_017022886.1:c.262G=	XP_016878375.1:p.Ala88=
NM_007074.4:c.262G= MANE Select	NP_009005.1:p.Ala88=
NM_001193333.3:c.262G=	NP_001180262.1:p.Ala88=