Canonical Allele Identifier: CA395493600

Gene: CORO1A

Linked Data

• MyVariant Identifiers: chr16:g.30198240C>G (hg19) ; chr16:g.30186919C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30186919C>G , CM000678.2:g.30186919C>G	GRCh38
NC_000016.9:g.30198240C>G , CM000678.1:g.30198240C>G	GRCh37
NC_000016.8:g.30105741C>G	NCBI36
NG_023415.1:g.8315C>G , LRG_195:g.8315C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696217.1:n.506C>G
ENST00000219150.10:c.425C>G MANE Select	ENSP00000219150.6:p.Thr142Arg
ENST00000219150.9:c.425C>G	ENSP00000219150.5:p.Thr142Arg
ENST00000561815.5:c.533C>G	ENSP00000456756.1:p.Thr178Arg
ENST00000563778.5:c.425C>G	ENSP00000456266.1:p.Thr142Arg
ENST00000564768.1:n.238C>G
ENST00000565497.5:c.425C>G	ENSP00000456457.1:p.Thr142Arg
ENST00000567034.5:n.893C>G
ENST00000568763.1:n.1737C>G
ENST00000568982.5:n.543C>G
ENST00000569203.5:c.425C>G	ENSP00000454752.1:p.Thr142Arg
ENST00000569469.1:n.432-120C>G
ENST00000569970.1:c.425C>G	ENSP00000457509.1:p.Thr142Arg
ENST00000570045.5:c.425C>G	ENSP00000455552.1:p.Thr142Arg
ENST00000570244.5:c.302C>G	ENSP00000457332.1:p.Thr101Arg
NM_001193333.2:c.425C>G	NP_001180262.1:p.Thr142Arg
NM_007074.3:c.425C>G	NP_009005.1:p.Thr142Arg
XM_011545714.1:c.425C>G	XP_011544016.1:p.Thr142Arg
XM_011545714.2:c.425C>G	XP_011544016.1:p.Thr142Arg
XM_017022885.2:c.425C>G	XP_016878374.1:p.Thr142Arg
XM_017022886.1:c.425C>G	XP_016878375.1:p.Thr142Arg
NM_007074.4:c.425C>G MANE Select	NP_009005.1:p.Thr142Arg
NM_001193333.3:c.425C>G	NP_001180262.1:p.Thr142Arg