Canonical Allele Identifier: CA2216454771

Gene: CORO1A

Linked Data

• ClinVar Variation Id: 2149228
• ClinVar RCV Id: RCV003065378
• dbSNP Id: rs2073339822
• gnomAD v4: 16-30186802-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30186802C>A , CM000678.2:g.30186802C>A	GRCh38
NC_000016.9:g.30198123C>A , CM000678.1:g.30198123C>A	GRCh37
NC_000016.8:g.30105624C>A	NCBI36
NG_023415.1:g.8198C>A , LRG_195:g.8198C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696217.1:n.389C>A
ENST00000219150.10:c.322-14C>A MANE Select	ENSP00000219150.6:n.322-14C>A
ENST00000219150.9:c.322-14C>A	ENSP00000219150.5:n.322-14C>A
ENST00000561815.5:c.430-14C>A	ENSP00000456756.1:n.430-14C>A
ENST00000563778.5:c.322-14C>A	ENSP00000456266.1:n.322-14C>A
ENST00000564768.1:n.121C>A
ENST00000565497.5:c.322-14C>A	ENSP00000456457.1:n.322-14C>A
ENST00000567034.5:n.790-14C>A
ENST00000568763.1:n.1634-14C>A
ENST00000568982.5:n.440-14C>A
ENST00000569203.5:c.322-14C>A	ENSP00000454752.1:n.322-14C>A
ENST00000569469.1:n.431+82C>A
ENST00000569970.1:c.322-14C>A	ENSP00000457509.1:n.322-14C>A
ENST00000570045.5:c.322-14C>A	ENSP00000455552.1:n.322-14C>A
ENST00000570244.5:c.199-14C>A	ENSP00000457332.1:n.199-14C>A
NM_001193333.2:c.322-14C>A	NP_001180262.1:n.322-14C>A
NM_007074.3:c.322-14C>A	NP_009005.1:n.322-14C>A
XM_011545714.1:c.322-14C>A	XP_011544016.1:n.322-14C>A
XM_011545714.2:c.322-14C>A	XP_011544016.1:n.322-14C>A
XM_017022885.2:c.322-14C>A	XP_016878374.1:n.322-14C>A
XM_017022886.1:c.322-14C>A	XP_016878375.1:n.322-14C>A
NM_007074.4:c.322-14C>A MANE Select	NP_009005.1:n.322-14C>A
NM_001193333.3:c.322-14C>A	NP_001180262.1:n.322-14C>A