Canonical Allele Identifier: CA622166876

Gene: CORO1A

Linked Data

• dbSNP Id: rs1376185247
• gnomAD v2: 16-30198079-CT-C
• gnomAD v4: 16-30186758-CT-C
• MyVariant Identifiers: chr16:g.30198080del (hg19) ; chr16:g.30186759del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30186759del , CM000678.2:g.30186759del	GRCh38
NC_000016.9:g.30198080del , CM000678.1:g.30198080del	GRCh37
NC_000016.8:g.30105581del	NCBI36
NG_023415.1:g.8155del , LRG_195:g.8155del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696217.1:n.346del
ENST00000219150.10:c.321+39del MANE Select	ENSP00000219150.6:n.321+39del
ENST00000219150.9:c.321+39del	ENSP00000219150.5:n.321+39del
ENST00000561815.5:c.429+39del	ENSP00000456756.1:n.429+39del
ENST00000563778.5:c.321+39del	ENSP00000456266.1:n.321+39del
ENST00000564768.1:n.78del
ENST00000565497.5:c.321+39del	ENSP00000456457.1:n.321+39del
ENST00000567034.5:n.789+39del
ENST00000568763.1:n.1633+39del
ENST00000568982.5:n.439+39del
ENST00000569203.5:c.321+39del	ENSP00000454752.1:n.321+39del
ENST00000569469.1:n.431+39del
ENST00000569970.1:c.321+39del	ENSP00000457509.1:n.321+39del
ENST00000570045.5:c.321+39del	ENSP00000455552.1:n.321+39del
ENST00000570244.5:c.199-57del	ENSP00000457332.1:n.199-57del
NM_001193333.2:c.321+39del	NP_001180262.1:n.321+39del
NM_007074.3:c.321+39del	NP_009005.1:n.321+39del
XM_011545714.1:c.321+39del	XP_011544016.1:n.321+39del
XM_011545714.2:c.321+39del	XP_011544016.1:n.321+39del
XM_017022885.2:c.321+39del	XP_016878374.1:n.321+39del
XM_017022886.1:c.321+39del	XP_016878375.1:n.321+39del
NM_007074.4:c.321+39del MANE Select	NP_009005.1:n.321+39del
NM_001193333.3:c.321+39del	NP_001180262.1:n.321+39del