Canonical Allele Identifier: CA2216454800

Gene: CORO1A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30186851C= , CM000678.2:g.30186851C=	GRCh38
NC_000016.9:g.30198172C= , CM000678.1:g.30198172C=	GRCh37
NC_000016.8:g.30105673C=	NCBI36
NG_023415.1:g.8247C= , LRG_195:g.8247C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696217.1:n.438C=
ENST00000219150.10:c.357C= MANE Select	ENSP00000219150.6:p.Pro119=
ENST00000219150.9:c.357C=	ENSP00000219150.5:p.Pro119=
ENST00000561815.5:c.465C=	ENSP00000456756.1:p.Pro155=
ENST00000563778.5:c.357C=	ENSP00000456266.1:p.Pro119=
ENST00000564768.1:n.170C=
ENST00000565497.5:c.357C=	ENSP00000456457.1:p.Pro119=
ENST00000567034.5:n.825C=
ENST00000568763.1:n.1669C=
ENST00000568982.5:n.475C=
ENST00000569203.5:c.357C=	ENSP00000454752.1:p.Pro119=
ENST00000569469.1:n.431+131C=
ENST00000569970.1:c.357C=	ENSP00000457509.1:p.Pro119=
ENST00000570045.5:c.357C=	ENSP00000455552.1:p.Pro119=
ENST00000570244.5:c.234C=	ENSP00000457332.1:p.Pro78=
NM_001193333.2:c.357C=	NP_001180262.1:p.Pro119=
NM_007074.3:c.357C=	NP_009005.1:p.Pro119=
XM_011545714.1:c.357C=	XP_011544016.1:p.Pro119=
XM_011545714.2:c.357C=	XP_011544016.1:p.Pro119=
XM_017022885.2:c.357C=	XP_016878374.1:p.Pro119=
XM_017022886.1:c.357C=	XP_016878375.1:p.Pro119=
NM_007074.4:c.357C= MANE Select	NP_009005.1:p.Pro119=
NM_001193333.3:c.357C=	NP_001180262.1:p.Pro119=