Canonical Allele Identifier: CA395493787

Gene: CORO1A

Linked Data

• gnomAD v4: 16-30186943-C-T
• MyVariant Identifiers: chr16:g.30198264C>T (hg19) ; chr16:g.30186943C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30186943C>T , CM000678.2:g.30186943C>T	GRCh38
NC_000016.9:g.30198264C>T , CM000678.1:g.30198264C>T	GRCh37
NC_000016.8:g.30105765C>T	NCBI36
NG_023415.1:g.8339C>T , LRG_195:g.8339C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696217.1:n.530C>T
ENST00000219150.10:c.449C>T MANE Select	ENSP00000219150.6:p.Ala150Val
ENST00000219150.9:c.449C>T	ENSP00000219150.5:p.Ala150Val
ENST00000561815.5:c.557C>T	ENSP00000456756.1:p.Ala186Val
ENST00000563778.5:c.449C>T	ENSP00000456266.1:p.Ala150Val
ENST00000564768.1:n.262C>T
ENST00000565497.5:c.449C>T	ENSP00000456457.1:p.Ala150Val
ENST00000567034.5:n.917C>T
ENST00000568763.1:n.1761C>T
ENST00000568982.5:n.567C>T
ENST00000569469.1:n.432-96C>T
ENST00000569970.1:c.449C>T	ENSP00000457509.1:p.Ala150Val
ENST00000570045.5:c.449C>T	ENSP00000455552.1:p.Ala150Val
ENST00000570244.5:c.326C>T	ENSP00000457332.1:p.Ala109Val
NM_001193333.2:c.449C>T	NP_001180262.1:p.Ala150Val
NM_007074.3:c.449C>T	NP_009005.1:p.Ala150Val
XM_011545714.1:c.449C>T	XP_011544016.1:p.Ala150Val
XM_011545714.2:c.449C>T	XP_011544016.1:p.Ala150Val
XM_017022885.2:c.449C>T	XP_016878374.1:p.Ala150Val
XM_017022886.1:c.449C>T	XP_016878375.1:p.Ala150Val
NM_007074.4:c.449C>T MANE Select	NP_009005.1:p.Ala150Val
NM_001193333.3:c.449C>T	NP_001180262.1:p.Ala150Val