Canonical Allele Identifier: CA395493435

Gene: CORO1A

Linked Data

• dbSNP Id: rs1350063119
• gnomAD v2: 16-30198221-A-G
• gnomAD v4: 16-30186900-A-G
• MyVariant Identifiers: chr16:g.30198221A>G (hg19) ; chr16:g.30186900A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30186900A>G , CM000678.2:g.30186900A>G	GRCh38
NC_000016.9:g.30198221A>G , CM000678.1:g.30198221A>G	GRCh37
NC_000016.8:g.30105722A>G	NCBI36
NG_023415.1:g.8296A>G , LRG_195:g.8296A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696217.1:n.487A>G
ENST00000219150.10:c.406A>G MANE Select	ENSP00000219150.6:p.Ile136Val
ENST00000219150.9:c.406A>G	ENSP00000219150.5:p.Ile136Val
ENST00000561815.5:c.514A>G	ENSP00000456756.1:p.Ile172Val
ENST00000563778.5:c.406A>G	ENSP00000456266.1:p.Ile136Val
ENST00000564768.1:n.219A>G
ENST00000565497.5:c.406A>G	ENSP00000456457.1:p.Ile136Val
ENST00000567034.5:n.874A>G
ENST00000568763.1:n.1718A>G
ENST00000568982.5:n.524A>G
ENST00000569203.5:c.406A>G	ENSP00000454752.1:p.Ile136Val
ENST00000569469.1:n.432-139A>G
ENST00000569970.1:c.406A>G	ENSP00000457509.1:p.Ile136Val
ENST00000570045.5:c.406A>G	ENSP00000455552.1:p.Ile136Val
ENST00000570244.5:c.283A>G	ENSP00000457332.1:p.Ile95Val
NM_001193333.2:c.406A>G	NP_001180262.1:p.Ile136Val
NM_007074.3:c.406A>G	NP_009005.1:p.Ile136Val
XM_011545714.1:c.406A>G	XP_011544016.1:p.Ile136Val
XM_011545714.2:c.406A>G	XP_011544016.1:p.Ile136Val
XM_017022885.2:c.406A>G	XP_016878374.1:p.Ile136Val
XM_017022886.1:c.406A>G	XP_016878375.1:p.Ile136Val
NM_007074.4:c.406A>G MANE Select	NP_009005.1:p.Ile136Val
NM_001193333.3:c.406A>G	NP_001180262.1:p.Ile136Val