Canonical Allele Identifier: CA2216454581

Gene: CORO1A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30186407_30186428delinsCTGGGGTTTGCCCAGGCCATTT , CM000678.2:g.30186407_30186428delinsCTGGGGTTTGCCCAGGCCATTT	GRCh38
NC_000016.9:g.30197728_30197749delinsCTGGGGTTTGCCCAGGCCATTT , CM000678.1:g.30197728_30197749delinsCTGGGGTTTGCCCAGGCCATTT	GRCh37
NC_000016.8:g.30105229_30105250delinsCTGGGGTTTGCCCAGGCCATTT	NCBI36
NG_023415.1:g.7803_7824delinsCTGGGGTTTGCCCAGGCCATTT , LRG_195:g.7803_7824delinsCTGGGGTTTGCCCAGGCCATTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219150.10:c.199-191_199-170delinsCTGGGGTTTGCCCAGGCCATTT MANE Select	ENSP00000219150.6:n.199-191_199-170delinsCTGGGGTTTGCCCAGGCCAT...
ENST00000219150.9:c.199-191_199-170delinsCTGGGGTTTGCCCAGGCCATTT	ENSP00000219150.5:n.199-191_199-170delinsCTGGGGTTTGCCCAGGCCAT...
ENST00000561815.5:c.307-191_307-170delinsCTGGGGTTTGCCCAGGCCATTT	ENSP00000456756.1:n.307-191_307-170delinsCTGGGGTTTGCCCAGGCCAT...
ENST00000563778.5:c.199-191_199-170delinsCTGGGGTTTGCCCAGGCCATTT	ENSP00000456266.1:n.199-191_199-170delinsCTGGGGTTTGCCCAGGCCAT...
ENST00000565497.5:c.199-191_199-170delinsCTGGGGTTTGCCCAGGCCATTT	ENSP00000456457.1:n.199-191_199-170delinsCTGGGGTTTGCCCAGGCCAT...
ENST00000567034.5:n.476_497delinsCTGGGGTTTGCCCAGGCCATTT
ENST00000568763.1:n.1320_1341delinsCTGGGGTTTGCCCAGGCCATTT
ENST00000568982.5:n.317-191_317-170delinsCTGGGGTTTGCCCAGGCCATTT
ENST00000569203.5:c.199-191_199-170delinsCTGGGGTTTGCCCAGGCCATTT	ENSP00000454752.1:n.199-191_199-170delinsCTGGGGTTTGCCCAGGCCAT...
ENST00000569469.1:n.309-191_309-170delinsCTGGGGTTTGCCCAGGCCATTT
ENST00000569970.1:c.199-191_199-170delinsCTGGGGTTTGCCCAGGCCATTT	ENSP00000457509.1:n.199-191_199-170delinsCTGGGGTTTGCCCAGGCCAT...
ENST00000570045.5:c.199-191_199-170delinsCTGGGGTTTGCCCAGGCCATTT	ENSP00000455552.1:n.199-191_199-170delinsCTGGGGTTTGCCCAGGCCAT...
ENST00000570244.5:c.199-409_199-388delinsCTGGGGTTTGCCCAGGCCATTT	ENSP00000457332.1:n.199-409_199-388delinsCTGGGGTTTGCCCAGGCCAT...
NM_001193333.2:c.199-191_199-170delinsCTGGGGTTTGCCCAGGCCATTT	NP_001180262.1:n.199-191_199-170delinsCTGGGGTTTGCCCAGGCCATTT
NM_007074.3:c.199-191_199-170delinsCTGGGGTTTGCCCAGGCCATTT	NP_009005.1:n.199-191_199-170delinsCTGGGGTTTGCCCAGGCCATTT
XM_011545714.1:c.199-191_199-170delinsCTGGGGTTTGCCCAGGCCATTT	XP_011544016.1:n.199-191_199-170delinsCTGGGGTTTGCCCAGGCCATTT
XM_011545714.2:c.199-191_199-170delinsCTGGGGTTTGCCCAGGCCATTT	XP_011544016.1:n.199-191_199-170delinsCTGGGGTTTGCCCAGGCCATTT
XM_017022885.2:c.199-191_199-170delinsCTGGGGTTTGCCCAGGCCATTT	XP_016878374.1:n.199-191_199-170delinsCTGGGGTTTGCCCAGGCCATTT
XM_017022886.1:c.199-191_199-170delinsCTGGGGTTTGCCCAGGCCATTT	XP_016878375.1:n.199-191_199-170delinsCTGGGGTTTGCCCAGGCCATTT
NM_007074.4:c.199-191_199-170delinsCTGGGGTTTGCCCAGGCCATTT MANE Select	NP_009005.1:n.199-191_199-170delinsCTGGGGTTTGCCCAGGCCATTT
NM_001193333.3:c.199-191_199-170delinsCTGGGGTTTGCCCAGGCCATTT	NP_001180262.1:n.199-191_199-170delinsCTGGGGTTTGCCCAGGCCATTT