Canonical Allele Identifier: CA8003092

Gene: CORO1A

Linked Data

• dbSNP Id: rs756290143
• ExAC: 16:30198124 CCCT / C
• gnomAD v2: 16-30198124-CCCT-C
• gnomAD v4: 16-30186803-CCCT-C
• MyVariant Identifiers: chr16:g.30198125_30198127del (hg19) ; chr16:g.30186804_30186806del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30186808_30186810del , CM000678.2:g.30186808_30186810del	GRCh38
NC_000016.9:g.30198129_30198131del , CM000678.1:g.30198129_30198131del	GRCh37
NC_000016.8:g.30105630_30105632del	NCBI36
NG_023415.1:g.8204_8206del , LRG_195:g.8204_8206del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696217.1:n.395_397del
ENST00000219150.10:c.322-8_322-6del MANE Select	ENSP00000219150.6:n.322-8_322-6del
ENST00000219150.9:c.322-8_322-6del	ENSP00000219150.5:n.322-8_322-6del
ENST00000561815.5:c.430-8_430-6del	ENSP00000456756.1:n.430-8_430-6del
ENST00000563778.5:c.322-8_322-6del	ENSP00000456266.1:n.322-8_322-6del
ENST00000564768.1:n.127_129del
ENST00000565497.5:c.322-8_322-6del	ENSP00000456457.1:n.322-8_322-6del
ENST00000567034.5:n.790-8_790-6del
ENST00000568763.1:n.1634-8_1634-6del
ENST00000568982.5:n.440-8_440-6del
ENST00000569203.5:c.322-8_322-6del	ENSP00000454752.1:n.322-8_322-6del
ENST00000569469.1:n.431+88_431+90del
ENST00000569970.1:c.322-8_322-6del	ENSP00000457509.1:n.322-8_322-6del
ENST00000570045.5:c.322-8_322-6del	ENSP00000455552.1:n.322-8_322-6del
ENST00000570244.5:c.199-8_199-6del	ENSP00000457332.1:n.199-8_199-6del
NM_001193333.2:c.322-8_322-6del	NP_001180262.1:n.322-8_322-6del
NM_007074.3:c.322-8_322-6del	NP_009005.1:n.322-8_322-6del
XM_011545714.1:c.322-8_322-6del	XP_011544016.1:n.322-8_322-6del
XM_011545714.2:c.322-8_322-6del	XP_011544016.1:n.322-8_322-6del
XM_017022885.2:c.322-8_322-6del	XP_016878374.1:n.322-8_322-6del
XM_017022886.1:c.322-8_322-6del	XP_016878375.1:n.322-8_322-6del
NM_007074.4:c.322-8_322-6del MANE Select	NP_009005.1:n.322-8_322-6del
NM_001193333.3:c.322-8_322-6del	NP_001180262.1:n.322-8_322-6del