Canonical Allele Identifier: CA395493280

Gene: CORO1A

Linked Data

• gnomAD v4: 16-30186880-G-T
• MyVariant Identifiers: chr16:g.30198201G>T (hg19) ; chr16:g.30186880G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30186880G>T , CM000678.2:g.30186880G>T	GRCh38
NC_000016.9:g.30198201G>T , CM000678.1:g.30198201G>T	GRCh37
NC_000016.8:g.30105702G>T	NCBI36
NG_023415.1:g.8276G>T , LRG_195:g.8276G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696217.1:n.467G>T
ENST00000219150.10:c.386G>T MANE Select	ENSP00000219150.6:p.Gly129Val
ENST00000219150.9:c.386G>T	ENSP00000219150.5:p.Gly129Val
ENST00000561815.5:c.494G>T	ENSP00000456756.1:p.Gly165Val
ENST00000563778.5:c.386G>T	ENSP00000456266.1:p.Gly129Val
ENST00000564768.1:n.199G>T
ENST00000565497.5:c.386G>T	ENSP00000456457.1:p.Gly129Val
ENST00000567034.5:n.854G>T
ENST00000568763.1:n.1698G>T
ENST00000568982.5:n.504G>T
ENST00000569203.5:c.386G>T	ENSP00000454752.1:p.Gly129Val
ENST00000569469.1:n.432-159G>T
ENST00000569970.1:c.386G>T	ENSP00000457509.1:p.Gly129Val
ENST00000570045.5:c.386G>T	ENSP00000455552.1:p.Gly129Val
ENST00000570244.5:c.263G>T	ENSP00000457332.1:p.Gly88Val
NM_001193333.2:c.386G>T	NP_001180262.1:p.Gly129Val
NM_007074.3:c.386G>T	NP_009005.1:p.Gly129Val
XM_011545714.1:c.386G>T	XP_011544016.1:p.Gly129Val
XM_011545714.2:c.386G>T	XP_011544016.1:p.Gly129Val
XM_017022885.2:c.386G>T	XP_016878374.1:p.Gly129Val
XM_017022886.1:c.386G>T	XP_016878375.1:p.Gly129Val
NM_007074.4:c.386G>T MANE Select	NP_009005.1:p.Gly129Val
NM_001193333.3:c.386G>T	NP_001180262.1:p.Gly129Val