Canonical Allele Identifier: CA8003069
Gene: CORO1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1053147
ClinVar RCV Id: RCV001361456
dbSNP Id: rs773962517

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.30186671C>T , CM000678.2:g.30186671C>T GRCh38
NC_000016.9:g.30197992C>T , CM000678.1:g.30197992C>T GRCh37
NC_000016.8:g.30105493C>T NCBI36
NG_023415.1:g.8067C>T , LRG_195:g.8067C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000696217.1:n.258C>T
ENST00000219150.10:c.272C>T MANE Select ENSP00000219150.6:p.Pro91Leu
ENST00000219150.9:c.272C>T ENSP00000219150.5:p.Pro91Leu
ENST00000561815.5:c.380C>T ENSP00000456756.1:p.Pro127Leu
ENST00000563778.5:c.272C>T ENSP00000456266.1:p.Pro91Leu
ENST00000565497.5:c.272C>T ENSP00000456457.1:p.Pro91Leu
ENST00000567034.5:n.740C>T
ENST00000568763.1:n.1584C>T
ENST00000568982.5:n.390C>T
ENST00000569203.5:c.272C>T ENSP00000454752.1:p.Pro91Leu
ENST00000569469.1:n.382C>T
ENST00000569970.1:c.272C>T ENSP00000457509.1:p.Pro91Leu
ENST00000570045.5:c.272C>T ENSP00000455552.1:p.Pro91Leu
ENST00000570244.5:c.199-145C>T ENSP00000457332.1:n.199-145C>T
NM_001193333.2:c.272C>T NP_001180262.1:p.Pro91Leu
NM_007074.3:c.272C>T NP_009005.1:p.Pro91Leu
XM_011545714.1:c.272C>T XP_011544016.1:p.Pro91Leu
XM_011545714.2:c.272C>T XP_011544016.1:p.Pro91Leu
XM_017022885.2:c.272C>T XP_016878374.1:p.Pro91Leu
XM_017022886.1:c.272C>T XP_016878375.1:p.Pro91Leu
NM_007074.4:c.272C>T MANE Select NP_009005.1:p.Pro91Leu
NM_001193333.3:c.272C>T NP_001180262.1:p.Pro91Leu