Canonical Allele Identifier: CA2632684487

Gene: CORO1A

Linked Data

• gnomAD v4: 16-30186926-GA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30186928del , CM000678.2:g.30186928del	GRCh38
NC_000016.9:g.30198249del , CM000678.1:g.30198249del	GRCh37
NC_000016.8:g.30105750del	NCBI36
NG_023415.1:g.8324del , LRG_195:g.8324del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696217.1:n.515del
ENST00000219150.10:c.434del MANE Select	ENSP00000219150.6:p.Asn145ThrfsTer11
ENST00000219150.9:c.434del	ENSP00000219150.5:p.Asn145ThrfsTer11
ENST00000561815.5:c.542del	ENSP00000456756.1:p.Asn181ThrfsTer11
ENST00000563778.5:c.434del	ENSP00000456266.1:p.Asn145ThrfsTer11
ENST00000564768.1:n.247del
ENST00000565497.5:c.434del	ENSP00000456457.1:p.Asn145ThrfsTer11
ENST00000567034.5:n.902del
ENST00000568763.1:n.1746del
ENST00000568982.5:n.552del
ENST00000569203.5:c.434del	ENSP00000454752.1:p.Asn145ThrfsTer?
ENST00000569469.1:n.432-111del
ENST00000569970.1:c.434del	ENSP00000457509.1:p.Asn145ThrfsTer11
ENST00000570045.5:c.434del	ENSP00000455552.1:p.Asn145ThrfsTer11
ENST00000570244.5:c.311del	ENSP00000457332.1:p.Asn104ThrfsTer11
NM_001193333.2:c.434del	NP_001180262.1:p.Asn145ThrfsTer11
NM_007074.3:c.434del	NP_009005.1:p.Asn145ThrfsTer11
XM_011545714.1:c.434del	XP_011544016.1:p.Asn145ThrfsTer11
XM_011545714.2:c.434del	XP_011544016.1:p.Asn145ThrfsTer11
XM_017022885.2:c.434del	XP_016878374.1:p.Asn145ThrfsTer11
XM_017022886.1:c.434del	XP_016878375.1:p.Asn145ThrfsTer11
NM_007074.4:c.434del MANE Select	NP_009005.1:p.Asn145ThrfsTer11
NM_001193333.3:c.434del	NP_001180262.1:p.Asn145ThrfsTer11