Canonical Allele Identifier: CA2632683931

Gene: CORO1A

Linked Data

• gnomAD v4: 16-30186592-C-CT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30186595dup , CM000678.2:g.30186595dup	GRCh38
NC_000016.9:g.30197916dup , CM000678.1:g.30197916dup	GRCh37
NC_000016.8:g.30105417dup	NCBI36
NG_023415.1:g.7991dup , LRG_195:g.7991dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696217.1:n.182dup
ENST00000219150.10:c.199-3dup MANE Select	ENSP00000219150.6:n.199-3dup
ENST00000219150.9:c.199-3dup	ENSP00000219150.5:n.199-3dup
ENST00000561815.5:c.307-3dup	ENSP00000456756.1:n.307-3dup
ENST00000563778.5:c.199-3dup	ENSP00000456266.1:n.199-3dup
ENST00000565497.5:c.199-3dup	ENSP00000456457.1:n.199-3dup
ENST00000567034.5:n.664dup
ENST00000568763.1:n.1508dup
ENST00000568982.5:n.317-3dup
ENST00000569203.5:c.199-3dup	ENSP00000454752.1:n.199-3dup
ENST00000569469.1:n.309-3dup
ENST00000569970.1:c.199-3dup	ENSP00000457509.1:n.199-3dup
ENST00000570045.5:c.199-3dup	ENSP00000455552.1:n.199-3dup
ENST00000570244.5:c.199-221dup	ENSP00000457332.1:n.199-221dup
NM_001193333.2:c.199-3dup	NP_001180262.1:n.199-3dup
NM_007074.3:c.199-3dup	NP_009005.1:n.199-3dup
XM_011545714.1:c.199-3dup	XP_011544016.1:n.199-3dup
XM_011545714.2:c.199-3dup	XP_011544016.1:n.199-3dup
XM_017022885.2:c.199-3dup	XP_016878374.1:n.199-3dup
XM_017022886.1:c.199-3dup	XP_016878375.1:n.199-3dup
NM_007074.4:c.199-3dup MANE Select	NP_009005.1:n.199-3dup
NM_001193333.3:c.199-3dup	NP_001180262.1:n.199-3dup