Canonical Allele Identifier: CA2909493

Gene: CORIN

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.47643167T>A , CM000666.2:g.47643167T>A	GRCh38
NC_000004.11:g.47645184T>A , CM000666.1:g.47645184T>A	GRCh37
NC_000004.10:g.47339941T>A	NCBI36
NG_032679.1:g.199876A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273857.9:c.2047A>T MANE Select	ENSP00000273857.4:p.Ser683Cys
ENST00000273857.8:c.2047A>T	ENSP00000273857.4:p.Ser683Cys
ENST00000502252.5:c.1846A>T	ENSP00000424212.1:p.Ser616Cys
ENST00000504584.1:c.1936A>T	ENSP00000423216.1:p.Ser646Cys
ENST00000505754.1:n.354A>T
ENST00000505909.5:c.1936A>T	ENSP00000425401.1:p.Ser646Cys
ENST00000508498.5:c.1630A>T	ENSP00000425597.1:p.Ser544Cys
ENST00000610355.4:c.1735A>T	ENSP00000484087.1:p.Ser579Cys
NM_001278585.1:c.1735A>T	NP_001265514.1:p.Ser579Cys
NM_001278586.1:c.1936A>T	NP_001265515.1:p.Ser646Cys
NM_006587.3:c.2047A>T	NP_006578.2:p.Ser683Cys
XR_925283.1:n.87-819T>A
XR_925283.2:n.99-819T>A
NM_006587.4:c.2047A>T MANE Select	NP_006578.2:p.Ser683Cys
NM_001278586.2:c.1936A>T	NP_001265515.1:p.Ser646Cys
NM_001278585.2:c.1735A>T	NP_001265514.1:p.Ser579Cys