Canonical Allele Identifier: CA2841322372
Gene: CORO1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.30186924del , CM000678.2:g.30186924del GRCh38
NC_000016.9:g.30198245del , CM000678.1:g.30198245del GRCh37
NC_000016.8:g.30105746del NCBI36
NG_023415.1:g.8320del , LRG_195:g.8320del

Transcript Alleles

HGVS Amino-acid Change
ENST00000696217.1:n.511del
ENST00000219150.10:c.430del MANE Select ENSP00000219150.6:p.Gln144ArgfsTer12
ENST00000219150.9:c.430del ENSP00000219150.5:p.Gln144ArgfsTer12
ENST00000561815.5:c.538del ENSP00000456756.1:p.Gln180ArgfsTer12
ENST00000563778.5:c.430del ENSP00000456266.1:p.Gln144ArgfsTer12
ENST00000564768.1:n.243del
ENST00000565497.5:c.430del ENSP00000456457.1:p.Gln144ArgfsTer12
ENST00000567034.5:n.898del
ENST00000568763.1:n.1742del
ENST00000568982.5:n.548del
ENST00000569203.5:c.430del ENSP00000454752.1:p.Gln144ArgfsTer?
ENST00000569469.1:n.432-115del
ENST00000569970.1:c.430del ENSP00000457509.1:p.Gln144ArgfsTer12
ENST00000570045.5:c.430del ENSP00000455552.1:p.Gln144ArgfsTer12
ENST00000570244.5:c.307del ENSP00000457332.1:p.Gln103ArgfsTer12
NM_001193333.2:c.430del NP_001180262.1:p.Gln144ArgfsTer12
NM_007074.3:c.430del NP_009005.1:p.Gln144ArgfsTer12
XM_011545714.1:c.430del XP_011544016.1:p.Gln144ArgfsTer12
XM_011545714.2:c.430del XP_011544016.1:p.Gln144ArgfsTer12
XM_017022885.2:c.430del XP_016878374.1:p.Gln144ArgfsTer12
XM_017022886.1:c.430del XP_016878375.1:p.Gln144ArgfsTer12
NM_007074.4:c.430del MANE Select NP_009005.1:p.Gln144ArgfsTer12
NM_001193333.3:c.430del NP_001180262.1:p.Gln144ArgfsTer12