Canonical Allele Identifier: CA144709
Gene: CORO1A HGNC NCBI

Linked Data

ClinVar Variation Id: 64645
ClinVar RCV Id: RCV000054815
dbSNP Id: rs397514755

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.30186894G>A , CM000678.2:g.30186894G>A GRCh38
NC_000016.9:g.30198215G>A , CM000678.1:g.30198215G>A GRCh37
NC_000016.8:g.30105716G>A NCBI36
NG_023415.1:g.8290G>A , LRG_195:g.8290G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000696217.1:n.481G>A
ENST00000219150.10:c.400G>A MANE Select ENSP00000219150.6:p.Val134Met
ENST00000219150.9:c.400G>A ENSP00000219150.5:p.Val134Met
ENST00000561815.5:c.508G>A ENSP00000456756.1:p.Val170Met
ENST00000563778.5:c.400G>A ENSP00000456266.1:p.Val134Met
ENST00000564768.1:n.213G>A
ENST00000565497.5:c.400G>A ENSP00000456457.1:p.Val134Met
ENST00000567034.5:n.868G>A
ENST00000568763.1:n.1712G>A
ENST00000568982.5:n.518G>A
ENST00000569203.5:c.400G>A ENSP00000454752.1:p.Val134Met
ENST00000569469.1:n.432-145G>A
ENST00000569970.1:c.400G>A ENSP00000457509.1:p.Val134Met
ENST00000570045.5:c.400G>A ENSP00000455552.1:p.Val134Met
ENST00000570244.5:c.277G>A ENSP00000457332.1:p.Val93Met
NM_001193333.2:c.400G>A NP_001180262.1:p.Val134Met
NM_007074.3:c.400G>A NP_009005.1:p.Val134Met
XM_011545714.1:c.400G>A XP_011544016.1:p.Val134Met
XM_011545714.2:c.400G>A XP_011544016.1:p.Val134Met
XM_017022885.2:c.400G>A XP_016878374.1:p.Val134Met
XM_017022886.1:c.400G>A XP_016878375.1:p.Val134Met
NM_007074.4:c.400G>A MANE Select NP_009005.1:p.Val134Met
NM_001193333.3:c.400G>A NP_001180262.1:p.Val134Met