Canonical Allele Identifier: CA2909800

Gene: CORIN

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.47680192C>T , CM000666.2:g.47680192C>T	GRCh38
NC_000004.11:g.47682209C>T , CM000666.1:g.47682209C>T	GRCh37
NC_000004.10:g.47376966C>T	NCBI36
NG_032679.1:g.162851G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273857.9:c.1081G>A MANE Select	ENSP00000273857.4:p.Val361Met
ENST00000273857.8:c.1081G>A	ENSP00000273857.4:p.Val361Met
ENST00000502252.5:c.880G>A	ENSP00000424212.1:p.Val294Met
ENST00000502726.5:n.4717G>A
ENST00000503821.5:n.1140-2138G>A
ENST00000504584.1:c.1022-2138G>A	ENSP00000423216.1:n.1022-2138G>A
ENST00000505909.5:c.1022-2138G>A	ENSP00000425401.1:n.1022-2138G>A
ENST00000508498.5:c.664G>A	ENSP00000425597.1:p.Val222Met
ENST00000610355.4:c.821-2138G>A	ENSP00000484087.1:n.821-2138G>A
NM_001278585.1:c.821-2138G>A	NP_001265514.1:n.821-2138G>A
NM_001278586.1:c.1022-2138G>A	NP_001265515.1:n.1022-2138G>A
NM_006587.3:c.1081G>A	NP_006578.2:p.Val361Met
NM_006587.4:c.1081G>A MANE Select	NP_006578.2:p.Val361Met
NM_001278586.2:c.1022-2138G>A	NP_001265515.1:n.1022-2138G>A
NM_001278585.2:c.821-2138G>A	NP_001265514.1:n.821-2138G>A