Canonical Allele Identifier: CA8003104
Gene: CORO1A HGNC NCBI

Linked Data

ClinVar Variation Id: 651336
ClinVar RCV Id: RCV000806671
dbSNP Id: rs779055659

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.30186856G>A , CM000678.2:g.30186856G>A GRCh38
NC_000016.9:g.30198177G>A , CM000678.1:g.30198177G>A GRCh37
NC_000016.8:g.30105678G>A NCBI36
NG_023415.1:g.8252G>A , LRG_195:g.8252G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000696217.1:n.443G>A
ENST00000219150.10:c.362G>A MANE Select ENSP00000219150.6:p.Arg121Gln
ENST00000219150.9:c.362G>A ENSP00000219150.5:p.Arg121Gln
ENST00000561815.5:c.470G>A ENSP00000456756.1:p.Arg157Gln
ENST00000563778.5:c.362G>A ENSP00000456266.1:p.Arg121Gln
ENST00000564768.1:n.175G>A
ENST00000565497.5:c.362G>A ENSP00000456457.1:p.Arg121Gln
ENST00000567034.5:n.830G>A
ENST00000568763.1:n.1674G>A
ENST00000568982.5:n.480G>A
ENST00000569203.5:c.362G>A ENSP00000454752.1:p.Arg121Gln
ENST00000569469.1:n.431+136G>A
ENST00000569970.1:c.362G>A ENSP00000457509.1:p.Arg121Gln
ENST00000570045.5:c.362G>A ENSP00000455552.1:p.Arg121Gln
ENST00000570244.5:c.239G>A ENSP00000457332.1:p.Arg80Gln
NM_001193333.2:c.362G>A NP_001180262.1:p.Arg121Gln
NM_007074.3:c.362G>A NP_009005.1:p.Arg121Gln
XM_011545714.1:c.362G>A XP_011544016.1:p.Arg121Gln
XM_011545714.2:c.362G>A XP_011544016.1:p.Arg121Gln
XM_017022885.2:c.362G>A XP_016878374.1:p.Arg121Gln
XM_017022886.1:c.362G>A XP_016878375.1:p.Arg121Gln
NM_007074.4:c.362G>A MANE Select NP_009005.1:p.Arg121Gln
NM_001193333.3:c.362G>A NP_001180262.1:p.Arg121Gln