Canonical Allele Identifier: CA2632683267

Gene: CORO1A

Linked Data

• gnomAD v4: 16-30186425-A-AT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30186429dup , CM000678.2:g.30186429dup	GRCh38
NC_000016.9:g.30197750dup , CM000678.1:g.30197750dup	GRCh37
NC_000016.8:g.30105251dup	NCBI36
NG_023415.1:g.7825dup , LRG_195:g.7825dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696217.1:n.16dup
ENST00000219150.10:c.199-169dup MANE Select	ENSP00000219150.6:n.199-169dup
ENST00000219150.9:c.199-169dup	ENSP00000219150.5:n.199-169dup
ENST00000561815.5:c.307-169dup	ENSP00000456756.1:n.307-169dup
ENST00000563778.5:c.199-169dup	ENSP00000456266.1:n.199-169dup
ENST00000565497.5:c.199-169dup	ENSP00000456457.1:n.199-169dup
ENST00000567034.5:n.498dup
ENST00000568763.1:n.1342dup
ENST00000568982.5:n.317-169dup
ENST00000569203.5:c.199-169dup	ENSP00000454752.1:n.199-169dup
ENST00000569469.1:n.309-169dup
ENST00000569970.1:c.199-169dup	ENSP00000457509.1:n.199-169dup
ENST00000570045.5:c.199-169dup	ENSP00000455552.1:n.199-169dup
ENST00000570244.5:c.199-387dup	ENSP00000457332.1:n.199-387dup
NM_001193333.2:c.199-169dup	NP_001180262.1:n.199-169dup
NM_007074.3:c.199-169dup	NP_009005.1:n.199-169dup
XM_011545714.1:c.199-169dup	XP_011544016.1:n.199-169dup
XM_011545714.2:c.199-169dup	XP_011544016.1:n.199-169dup
XM_017022885.2:c.199-169dup	XP_016878374.1:n.199-169dup
XM_017022886.1:c.199-169dup	XP_016878375.1:n.199-169dup
NM_007074.4:c.199-169dup MANE Select	NP_009005.1:n.199-169dup
NM_001193333.3:c.199-169dup	NP_001180262.1:n.199-169dup