Canonical Allele Identifier: CA719812508

Gene: CORO1A

Linked Data

• dbSNP Id: rs1172938502
• gnomAD v4: 16-30186453-A-ACCCGCC
• MyVariant Identifiers: chr16:g.30197774_30197775insCCCGCC (hg19) ; chr16:g.30186453_30186454insCCCGCC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30186458_30186463dup , CM000678.2:g.30186458_30186463dup	GRCh38
NC_000016.9:g.30197779_30197784dup , CM000678.1:g.30197779_30197784dup	GRCh37
NC_000016.8:g.30105280_30105285dup	NCBI36
NG_023415.1:g.7854_7859dup , LRG_195:g.7854_7859dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696217.1:n.45_50dup
ENST00000219150.10:c.199-140_199-135dup MANE Select	ENSP00000219150.6:n.199-140_199-135dup
ENST00000219150.9:c.199-140_199-135dup	ENSP00000219150.5:n.199-140_199-135dup
ENST00000561815.5:c.307-140_307-135dup	ENSP00000456756.1:n.307-140_307-135dup
ENST00000563778.5:c.199-140_199-135dup	ENSP00000456266.1:n.199-140_199-135dup
ENST00000565497.5:c.199-140_199-135dup	ENSP00000456457.1:n.199-140_199-135dup
ENST00000567034.5:n.527_532dup
ENST00000568763.1:n.1371_1376dup
ENST00000568982.5:n.317-140_317-135dup
ENST00000569203.5:c.199-140_199-135dup	ENSP00000454752.1:n.199-140_199-135dup
ENST00000569469.1:n.309-140_309-135dup
ENST00000569970.1:c.199-140_199-135dup	ENSP00000457509.1:n.199-140_199-135dup
ENST00000570045.5:c.199-140_199-135dup	ENSP00000455552.1:n.199-140_199-135dup
ENST00000570244.5:c.199-358_199-353dup	ENSP00000457332.1:n.199-358_199-353dup
NM_001193333.2:c.199-140_199-135dup	NP_001180262.1:n.199-140_199-135dup
NM_007074.3:c.199-140_199-135dup	NP_009005.1:n.199-140_199-135dup
XM_011545714.1:c.199-140_199-135dup	XP_011544016.1:n.199-140_199-135dup
XM_011545714.2:c.199-140_199-135dup	XP_011544016.1:n.199-140_199-135dup
XM_017022885.2:c.199-140_199-135dup	XP_016878374.1:n.199-140_199-135dup
XM_017022886.1:c.199-140_199-135dup	XP_016878375.1:n.199-140_199-135dup
NM_007074.4:c.199-140_199-135dup MANE Select	NP_009005.1:n.199-140_199-135dup
NM_001193333.3:c.199-140_199-135dup	NP_001180262.1:n.199-140_199-135dup