Canonical Allele Identifier: CA2216454647
Gene: CORO1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.30186550T= , CM000678.2:g.30186550T= GRCh38
NC_000016.9:g.30197871T= , CM000678.1:g.30197871T= GRCh37
NC_000016.8:g.30105372T= NCBI36
NG_023415.1:g.7946T= , LRG_195:g.7946T=

Transcript Alleles

HGVS Amino-acid change
ENST00000696217.1:n.137T=
ENST00000219150.10:c.199-48T= MANE Select ENSP00000219150.6:n.199-48T=
ENST00000219150.9:c.199-48T= ENSP00000219150.5:n.199-48T=
ENST00000561815.5:c.307-48T= ENSP00000456756.1:n.307-48T=
ENST00000563778.5:c.199-48T= ENSP00000456266.1:n.199-48T=
ENST00000565497.5:c.199-48T= ENSP00000456457.1:n.199-48T=
ENST00000567034.5:n.619T=
ENST00000568763.1:n.1463T=
ENST00000568982.5:n.317-48T=
ENST00000569203.5:c.199-48T= ENSP00000454752.1:n.199-48T=
ENST00000569469.1:n.309-48T=
ENST00000569970.1:c.199-48T= ENSP00000457509.1:n.199-48T=
ENST00000570045.5:c.199-48T= ENSP00000455552.1:n.199-48T=
ENST00000570244.5:c.199-266T= ENSP00000457332.1:n.199-266T=
NM_001193333.2:c.199-48T= NP_001180262.1:n.199-48T=
NM_007074.3:c.199-48T= NP_009005.1:n.199-48T=
XM_011545714.1:c.199-48T= XP_011544016.1:n.199-48T=
XM_011545714.2:c.199-48T= XP_011544016.1:n.199-48T=
XM_017022885.2:c.199-48T= XP_016878374.1:n.199-48T=
XM_017022886.1:c.199-48T= XP_016878375.1:n.199-48T=
NM_007074.4:c.199-48T= MANE Select NP_009005.1:n.199-48T=
NM_001193333.3:c.199-48T= NP_001180262.1:n.199-48T=