Canonical Allele Identifier: CA395493758

Gene: CORO1A

Linked Data

• gnomAD v4: 16-30186940-G-T
• MyVariant Identifiers: chr16:g.30198261G>T (hg19) ; chr16:g.30186940G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30186940G>T , CM000678.2:g.30186940G>T	GRCh38
NC_000016.9:g.30198261G>T , CM000678.1:g.30198261G>T	GRCh37
NC_000016.8:g.30105762G>T	NCBI36
NG_023415.1:g.8336G>T , LRG_195:g.8336G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696217.1:n.527G>T
ENST00000219150.10:c.446G>T MANE Select	ENSP00000219150.6:p.Ser149Ile
ENST00000219150.9:c.446G>T	ENSP00000219150.5:p.Ser149Ile
ENST00000561815.5:c.554G>T	ENSP00000456756.1:p.Ser185Ile
ENST00000563778.5:c.446G>T	ENSP00000456266.1:p.Ser149Ile
ENST00000564768.1:n.259G>T
ENST00000565497.5:c.446G>T	ENSP00000456457.1:p.Ser149Ile
ENST00000567034.5:n.914G>T
ENST00000568763.1:n.1758G>T
ENST00000568982.5:n.564G>T
ENST00000569469.1:n.432-99G>T
ENST00000569970.1:c.446G>T	ENSP00000457509.1:p.Ser149Ile
ENST00000570045.5:c.446G>T	ENSP00000455552.1:p.Ser149Ile
ENST00000570244.5:c.323G>T	ENSP00000457332.1:p.Ser108Ile
NM_001193333.2:c.446G>T	NP_001180262.1:p.Ser149Ile
NM_007074.3:c.446G>T	NP_009005.1:p.Ser149Ile
XM_011545714.1:c.446G>T	XP_011544016.1:p.Ser149Ile
XM_011545714.2:c.446G>T	XP_011544016.1:p.Ser149Ile
XM_017022885.2:c.446G>T	XP_016878374.1:p.Ser149Ile
XM_017022886.1:c.446G>T	XP_016878375.1:p.Ser149Ile
NM_007074.4:c.446G>T MANE Select	NP_009005.1:p.Ser149Ile
NM_001193333.3:c.446G>T	NP_001180262.1:p.Ser149Ile