Canonical Allele Identifier: CA8003103
Gene: CORO1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2308262
ClinVar RCV Id: RCV002900929
dbSNP Id: rs370896577

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.30186855C>T , CM000678.2:g.30186855C>T GRCh38
NC_000016.9:g.30198176C>T , CM000678.1:g.30198176C>T GRCh37
NC_000016.8:g.30105677C>T NCBI36
NG_023415.1:g.8251C>T , LRG_195:g.8251C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000696217.1:n.442C>T
ENST00000219150.10:c.361C>T MANE Select ENSP00000219150.6:p.Arg121Trp
ENST00000219150.9:c.361C>T ENSP00000219150.5:p.Arg121Trp
ENST00000561815.5:c.469C>T ENSP00000456756.1:p.Arg157Trp
ENST00000563778.5:c.361C>T ENSP00000456266.1:p.Arg121Trp
ENST00000564768.1:n.174C>T
ENST00000565497.5:c.361C>T ENSP00000456457.1:p.Arg121Trp
ENST00000567034.5:n.829C>T
ENST00000568763.1:n.1673C>T
ENST00000568982.5:n.479C>T
ENST00000569203.5:c.361C>T ENSP00000454752.1:p.Arg121Trp
ENST00000569469.1:n.431+135C>T
ENST00000569970.1:c.361C>T ENSP00000457509.1:p.Arg121Trp
ENST00000570045.5:c.361C>T ENSP00000455552.1:p.Arg121Trp
ENST00000570244.5:c.238C>T ENSP00000457332.1:p.Arg80Trp
NM_001193333.2:c.361C>T NP_001180262.1:p.Arg121Trp
NM_007074.3:c.361C>T NP_009005.1:p.Arg121Trp
XM_011545714.1:c.361C>T XP_011544016.1:p.Arg121Trp
XM_011545714.2:c.361C>T XP_011544016.1:p.Arg121Trp
XM_017022885.2:c.361C>T XP_016878374.1:p.Arg121Trp
XM_017022886.1:c.361C>T XP_016878375.1:p.Arg121Trp
NM_007074.4:c.361C>T MANE Select NP_009005.1:p.Arg121Trp
NM_001193333.3:c.361C>T NP_001180262.1:p.Arg121Trp