Canonical Allele Identifier: CA622166883

Gene: CORO1A

Linked Data

• dbSNP Id: rs1451230074
• gnomAD v2: 16-30198269-G-C
• gnomAD v4: 16-30186948-G-C
• MyVariant Identifiers: chr16:g.30198269G>C (hg19) ; chr16:g.30186948G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30186948G>C , CM000678.2:g.30186948G>C	GRCh38
NC_000016.9:g.30198269G>C , CM000678.1:g.30198269G>C	GRCh37
NC_000016.8:g.30105770G>C	NCBI36
NG_023415.1:g.8344G>C , LRG_195:g.8344G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696217.1:n.532+3G>C
ENST00000219150.10:c.451+3G>C MANE Select	ENSP00000219150.6:n.451+3G>C
ENST00000219150.9:c.451+3G>C	ENSP00000219150.5:n.451+3G>C
ENST00000561815.5:c.559+3G>C	ENSP00000456756.1:n.559+3G>C
ENST00000563778.5:c.451+3G>C	ENSP00000456266.1:n.451+3G>C
ENST00000564768.1:n.267G>C
ENST00000565497.5:c.451+3G>C	ENSP00000456457.1:n.451+3G>C
ENST00000567034.5:n.922G>C
ENST00000568763.1:n.1763+3G>C
ENST00000568982.5:n.572G>C
ENST00000569469.1:n.432-91G>C
ENST00000569970.1:c.451+3G>C	ENSP00000457509.1:n.451+3G>C
ENST00000570045.5:c.451+3G>C	ENSP00000455552.1:n.451+3G>C
ENST00000570244.5:c.328+3G>C	ENSP00000457332.1:n.328+3G>C
NM_001193333.2:c.451+3G>C	NP_001180262.1:n.451+3G>C
NM_007074.3:c.451+3G>C	NP_009005.1:n.451+3G>C
XM_011545714.1:c.451+3G>C	XP_011544016.1:n.451+3G>C
XM_011545714.2:c.451+3G>C	XP_011544016.1:n.451+3G>C
XM_017022885.2:c.451+3G>C	XP_016878374.1:n.451+3G>C
XM_017022886.1:c.451+3G>C	XP_016878375.1:n.451+3G>C
NM_007074.4:c.451+3G>C MANE Select	NP_009005.1:n.451+3G>C
NM_001193333.3:c.451+3G>C	NP_001180262.1:n.451+3G>C