Canonical Allele Identifier: CA395493153

Gene: CORO1A

Linked Data

• dbSNP Id: rs1456321543
• gnomAD v2: 16-30198186-T-C
• gnomAD v3: 16-30186865-T-C
• gnomAD v4: 16-30186865-T-C
• MyVariant Identifiers: chr16:g.30198186T>C (hg19) ; chr16:g.30186865T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30186865T>C , CM000678.2:g.30186865T>C	GRCh38
NC_000016.9:g.30198186T>C , CM000678.1:g.30198186T>C	GRCh37
NC_000016.8:g.30105687T>C	NCBI36
NG_023415.1:g.8261T>C , LRG_195:g.8261T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696217.1:n.452T>C
ENST00000219150.10:c.371T>C MANE Select	ENSP00000219150.6:p.Val124Ala
ENST00000219150.9:c.371T>C	ENSP00000219150.5:p.Val124Ala
ENST00000561815.5:c.479T>C	ENSP00000456756.1:p.Val160Ala
ENST00000563778.5:c.371T>C	ENSP00000456266.1:p.Val124Ala
ENST00000564768.1:n.184T>C
ENST00000565497.5:c.371T>C	ENSP00000456457.1:p.Val124Ala
ENST00000567034.5:n.839T>C
ENST00000568763.1:n.1683T>C
ENST00000568982.5:n.489T>C
ENST00000569203.5:c.371T>C	ENSP00000454752.1:p.Val124Ala
ENST00000569469.1:n.431+145T>C
ENST00000569970.1:c.371T>C	ENSP00000457509.1:p.Val124Ala
ENST00000570045.5:c.371T>C	ENSP00000455552.1:p.Val124Ala
ENST00000570244.5:c.248T>C	ENSP00000457332.1:p.Val83Ala
NM_001193333.2:c.371T>C	NP_001180262.1:p.Val124Ala
NM_007074.3:c.371T>C	NP_009005.1:p.Val124Ala
XM_011545714.1:c.371T>C	XP_011544016.1:p.Val124Ala
XM_011545714.2:c.371T>C	XP_011544016.1:p.Val124Ala
XM_017022885.2:c.371T>C	XP_016878374.1:p.Val124Ala
XM_017022886.1:c.371T>C	XP_016878375.1:p.Val124Ala
NM_007074.4:c.371T>C MANE Select	NP_009005.1:p.Val124Ala
NM_001193333.3:c.371T>C	NP_001180262.1:p.Val124Ala