Canonical Allele Identifier: CA2632684174

Gene: CORO1A

Linked Data

• gnomAD v4: 16-30186762-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30186762A>G , CM000678.2:g.30186762A>G	GRCh38
NC_000016.9:g.30198083A>G , CM000678.1:g.30198083A>G	GRCh37
NC_000016.8:g.30105584A>G	NCBI36
NG_023415.1:g.8158A>G , LRG_195:g.8158A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696217.1:n.349A>G
ENST00000219150.10:c.321+42A>G MANE Select	ENSP00000219150.6:n.321+42A>G
ENST00000219150.9:c.321+42A>G	ENSP00000219150.5:n.321+42A>G
ENST00000561815.5:c.429+42A>G	ENSP00000456756.1:n.429+42A>G
ENST00000563778.5:c.321+42A>G	ENSP00000456266.1:n.321+42A>G
ENST00000564768.1:n.81A>G
ENST00000565497.5:c.321+42A>G	ENSP00000456457.1:n.321+42A>G
ENST00000567034.5:n.789+42A>G
ENST00000568763.1:n.1633+42A>G
ENST00000568982.5:n.439+42A>G
ENST00000569203.5:c.321+42A>G	ENSP00000454752.1:n.321+42A>G
ENST00000569469.1:n.431+42A>G
ENST00000569970.1:c.321+42A>G	ENSP00000457509.1:n.321+42A>G
ENST00000570045.5:c.321+42A>G	ENSP00000455552.1:n.321+42A>G
ENST00000570244.5:c.199-54A>G	ENSP00000457332.1:n.199-54A>G
NM_001193333.2:c.321+42A>G	NP_001180262.1:n.321+42A>G
NM_007074.3:c.321+42A>G	NP_009005.1:n.321+42A>G
XM_011545714.1:c.321+42A>G	XP_011544016.1:n.321+42A>G
XM_011545714.2:c.321+42A>G	XP_011544016.1:n.321+42A>G
XM_017022885.2:c.321+42A>G	XP_016878374.1:n.321+42A>G
XM_017022886.1:c.321+42A>G	XP_016878375.1:n.321+42A>G
NM_007074.4:c.321+42A>G MANE Select	NP_009005.1:n.321+42A>G
NM_001193333.3:c.321+42A>G	NP_001180262.1:n.321+42A>G