Canonical Allele Identifier: CA395493776

Gene: CORO1A

Linked Data

• MyVariant Identifiers: chr16:g.30198262T>A (hg19) ; chr16:g.30186941T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30186941T>A , CM000678.2:g.30186941T>A	GRCh38
NC_000016.9:g.30198262T>A , CM000678.1:g.30198262T>A	GRCh37
NC_000016.8:g.30105763T>A	NCBI36
NG_023415.1:g.8337T>A , LRG_195:g.8337T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696217.1:n.528T>A
ENST00000219150.10:c.447T>A MANE Select	ENSP00000219150.6:p.Ser149Arg
ENST00000219150.9:c.447T>A	ENSP00000219150.5:p.Ser149Arg
ENST00000561815.5:c.555T>A	ENSP00000456756.1:p.Ser185Arg
ENST00000563778.5:c.447T>A	ENSP00000456266.1:p.Ser149Arg
ENST00000564768.1:n.260T>A
ENST00000565497.5:c.447T>A	ENSP00000456457.1:p.Ser149Arg
ENST00000567034.5:n.915T>A
ENST00000568763.1:n.1759T>A
ENST00000568982.5:n.565T>A
ENST00000569469.1:n.432-98T>A
ENST00000569970.1:c.447T>A	ENSP00000457509.1:p.Ser149Arg
ENST00000570045.5:c.447T>A	ENSP00000455552.1:p.Ser149Arg
ENST00000570244.5:c.324T>A	ENSP00000457332.1:p.Ser108Arg
NM_001193333.2:c.447T>A	NP_001180262.1:p.Ser149Arg
NM_007074.3:c.447T>A	NP_009005.1:p.Ser149Arg
XM_011545714.1:c.447T>A	XP_011544016.1:p.Ser149Arg
XM_011545714.2:c.447T>A	XP_011544016.1:p.Ser149Arg
XM_017022885.2:c.447T>A	XP_016878374.1:p.Ser149Arg
XM_017022886.1:c.447T>A	XP_016878375.1:p.Ser149Arg
NM_007074.4:c.447T>A MANE Select	NP_009005.1:p.Ser149Arg
NM_001193333.3:c.447T>A	NP_001180262.1:p.Ser149Arg