Canonical Allele Identifier: CA8003083

Gene: CORO1A

Linked Data

• dbSNP Id: rs553943700
• ExAC: 16:30198067 C / A
• gnomAD v2: 16-30198067-C-A
• gnomAD v3: 16-30186746-C-A
• gnomAD v4: 16-30186746-C-A
• MyVariant Identifiers: chr16:g.30198067C>A (hg19) ; chr16:g.30186746C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30186746C>A , CM000678.2:g.30186746C>A	GRCh38
NC_000016.9:g.30198067C>A , CM000678.1:g.30198067C>A	GRCh37
NC_000016.8:g.30105568C>A	NCBI36
NG_023415.1:g.8142C>A , LRG_195:g.8142C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696217.1:n.333C>A
ENST00000219150.10:c.321+26C>A MANE Select	ENSP00000219150.6:n.321+26C>A
ENST00000219150.9:c.321+26C>A	ENSP00000219150.5:n.321+26C>A
ENST00000561815.5:c.429+26C>A	ENSP00000456756.1:n.429+26C>A
ENST00000563778.5:c.321+26C>A	ENSP00000456266.1:n.321+26C>A
ENST00000564768.1:n.65C>A
ENST00000565497.5:c.321+26C>A	ENSP00000456457.1:n.321+26C>A
ENST00000567034.5:n.789+26C>A
ENST00000568763.1:n.1633+26C>A
ENST00000568982.5:n.439+26C>A
ENST00000569203.5:c.321+26C>A	ENSP00000454752.1:n.321+26C>A
ENST00000569469.1:n.431+26C>A
ENST00000569970.1:c.321+26C>A	ENSP00000457509.1:n.321+26C>A
ENST00000570045.5:c.321+26C>A	ENSP00000455552.1:n.321+26C>A
ENST00000570244.5:c.199-70C>A	ENSP00000457332.1:n.199-70C>A
NM_001193333.2:c.321+26C>A	NP_001180262.1:n.321+26C>A
NM_007074.3:c.321+26C>A	NP_009005.1:n.321+26C>A
XM_011545714.1:c.321+26C>A	XP_011544016.1:n.321+26C>A
XM_011545714.2:c.321+26C>A	XP_011544016.1:n.321+26C>A
XM_017022885.2:c.321+26C>A	XP_016878374.1:n.321+26C>A
XM_017022886.1:c.321+26C>A	XP_016878375.1:n.321+26C>A
NM_007074.4:c.321+26C>A MANE Select	NP_009005.1:n.321+26C>A
NM_001193333.3:c.321+26C>A	NP_001180262.1:n.321+26C>A