Canonical Allele Identifier: CA1410883192

Gene: CLRN1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.150927973G= , CM000665.2:g.150927973G=	GRCh38
NC_000003.11:g.150645760G= , CM000665.1:g.150645760G=	GRCh37
NC_000003.10:g.152128450G=	NCBI36
NG_009168.1:g.50027C= , LRG_700:g.50027C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327047.6:c.662C= MANE Select	ENSP00000322280.1:p.Ala221=
ENST00000295911.6:c.342+92C=	ENSP00000295911.2:n.342+92C=
ENST00000327047.5:c.662C=	ENSP00000322280.1:p.Ala221=
ENST00000328863.8:c.701C=	ENSP00000329158.4:p.Ala234=
ENST00000562308.5:c.104+13609C=
ENST00000565169.1:c.162+13609C=
ENST00000569170.5:c.162+13609C=
NM_001195794.1:c.701C= , LRG_700t1:c.701C=	NP_001182723.1:p.Ala234=
NM_001256819.1:c.*276C=	NP_001243748.1:n.*276C=
NM_052995.2:c.342+92C= , LRG_700t2:c.342+92C=	NP_443721.1:n.342+92C=
NM_174878.2:c.662C=	NP_777367.1:p.Ala221=
NR_046380.2:n.1143C=
XR_924167.1:n.974C=
NM_001256819.2:c.*276C=	NP_001243748.1:n.*276C=
NM_174878.3:c.662C= MANE Select	NP_777367.1:p.Ala221=
NR_046380.3:n.871C=