Canonical Allele Identifier: CA494892476

Gene: CORO1A

Linked Data

• gnomAD v4: 16-30186932-G-C
• MyVariant Identifiers: chr16:g.30198253G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30186932G>C , CM000678.2:g.30186932G>C	GRCh38
NC_000016.9:g.30198253G>C , CM000678.1:g.30198253G>C	GRCh37
NC_000016.8:g.30105754G>C	NCBI36
NG_023415.1:g.8328G>C , LRG_195:g.8328G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696217.1:n.519G>C
ENST00000219150.10:c.438G>C MANE Select	ENSP00000219150.6:p.Val146=
ENST00000219150.9:c.438G>C	ENSP00000219150.5:p.Val146=
ENST00000561815.5:c.546G>C	ENSP00000456756.1:p.Val182=
ENST00000563778.5:c.438G>C	ENSP00000456266.1:p.Val146=
ENST00000564768.1:n.251G>C
ENST00000565497.5:c.438G>C	ENSP00000456457.1:p.Val146=
ENST00000567034.5:n.906G>C
ENST00000568763.1:n.1750G>C
ENST00000568982.5:n.556G>C
ENST00000569203.5:c.438G>C	ENSP00000454752.1:p.Val146=
ENST00000569469.1:n.432-107G>C
ENST00000569970.1:c.438G>C	ENSP00000457509.1:p.Val146=
ENST00000570045.5:c.438G>C	ENSP00000455552.1:p.Val146=
ENST00000570244.5:c.315G>C	ENSP00000457332.1:p.Val105=
NM_001193333.2:c.438G>C	NP_001180262.1:p.Val146=
NM_007074.3:c.438G>C	NP_009005.1:p.Val146=
XM_011545714.1:c.438G>C	XP_011544016.1:p.Val146=
XM_011545714.2:c.438G>C	XP_011544016.1:p.Val146=
XM_017022885.2:c.438G>C	XP_016878374.1:p.Val146=
XM_017022886.1:c.438G>C	XP_016878375.1:p.Val146=
NM_007074.4:c.438G>C MANE Select	NP_009005.1:p.Val146=
NM_001193333.3:c.438G>C	NP_001180262.1:p.Val146=