Canonical Allele Identifier: CA395492168

Gene: CORO1A

Linked Data

• MyVariant Identifiers: chr16:g.30197987G>A (hg19) ; chr16:g.30186666G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30186666G>A , CM000678.2:g.30186666G>A	GRCh38
NC_000016.9:g.30197987G>A , CM000678.1:g.30197987G>A	GRCh37
NC_000016.8:g.30105488G>A	NCBI36
NG_023415.1:g.8062G>A , LRG_195:g.8062G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696217.1:n.253G>A
ENST00000219150.10:c.267G>A MANE Select	ENSP00000219150.6:p.Trp89Ter
ENST00000219150.9:c.267G>A	ENSP00000219150.5:p.Trp89Ter
ENST00000561815.5:c.375G>A	ENSP00000456756.1:p.Trp125Ter
ENST00000563778.5:c.267G>A	ENSP00000456266.1:p.Trp89Ter
ENST00000565497.5:c.267G>A	ENSP00000456457.1:p.Trp89Ter
ENST00000567034.5:n.735G>A
ENST00000568763.1:n.1579G>A
ENST00000568982.5:n.385G>A
ENST00000569203.5:c.267G>A	ENSP00000454752.1:p.Trp89Ter
ENST00000569469.1:n.377G>A
ENST00000569970.1:c.267G>A	ENSP00000457509.1:p.Trp89Ter
ENST00000570045.5:c.267G>A	ENSP00000455552.1:p.Trp89Ter
ENST00000570244.5:c.199-150G>A	ENSP00000457332.1:n.199-150G>A
NM_001193333.2:c.267G>A	NP_001180262.1:p.Trp89Ter
NM_007074.3:c.267G>A	NP_009005.1:p.Trp89Ter
XM_011545714.1:c.267G>A	XP_011544016.1:p.Trp89Ter
XM_011545714.2:c.267G>A	XP_011544016.1:p.Trp89Ter
XM_017022885.2:c.267G>A	XP_016878374.1:p.Trp89Ter
XM_017022886.1:c.267G>A	XP_016878375.1:p.Trp89Ter
NM_007074.4:c.267G>A MANE Select	NP_009005.1:p.Trp89Ter
NM_001193333.3:c.267G>A	NP_001180262.1:p.Trp89Ter