Canonical Allele Identifier: CA2216454831

Gene: CORO1A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30186920A= , CM000678.2:g.30186920A=	GRCh38
NC_000016.9:g.30198241A= , CM000678.1:g.30198241A=	GRCh37
NC_000016.8:g.30105742A=	NCBI36
NG_023415.1:g.8316A= , LRG_195:g.8316A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696217.1:n.507A=
ENST00000219150.10:c.426A= MANE Select	ENSP00000219150.6:p.Thr142=
ENST00000219150.9:c.426A=	ENSP00000219150.5:p.Thr142=
ENST00000561815.5:c.534A=	ENSP00000456756.1:p.Thr178=
ENST00000563778.5:c.426A=	ENSP00000456266.1:p.Thr142=
ENST00000564768.1:n.239A=
ENST00000565497.5:c.426A=	ENSP00000456457.1:p.Thr142=
ENST00000567034.5:n.894A=
ENST00000568763.1:n.1738A=
ENST00000568982.5:n.544A=
ENST00000569203.5:c.426A=	ENSP00000454752.1:p.Thr142=
ENST00000569469.1:n.432-119A=
ENST00000569970.1:c.426A=	ENSP00000457509.1:p.Thr142=
ENST00000570045.5:c.426A=	ENSP00000455552.1:p.Thr142=
ENST00000570244.5:c.303A=	ENSP00000457332.1:p.Thr101=
NM_001193333.2:c.426A=	NP_001180262.1:p.Thr142=
NM_007074.3:c.426A=	NP_009005.1:p.Thr142=
XM_011545714.1:c.426A=	XP_011544016.1:p.Thr142=
XM_011545714.2:c.426A=	XP_011544016.1:p.Thr142=
XM_017022885.2:c.426A=	XP_016878374.1:p.Thr142=
XM_017022886.1:c.426A=	XP_016878375.1:p.Thr142=
NM_007074.4:c.426A= MANE Select	NP_009005.1:p.Thr142=
NM_001193333.3:c.426A=	NP_001180262.1:p.Thr142=