Canonical Allele Identifier: CA1410882614

Gene: CLRN1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.150926686G= , CM000665.2:g.150926686G=	GRCh38
NC_000003.11:g.150644473G= , CM000665.1:g.150644473G=	GRCh37
NC_000003.10:g.152127163G=	NCBI36
NG_009168.1:g.51314C= , LRG_700:g.51314C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000327047.6:c.*1250C= MANE Select	ENSP00000322280.1:n.*1250C=
ENST00000295911.6:c.*166C=	ENSP00000295911.2:n.*166C=
ENST00000327047.5:c.*1250C=	ENSP00000322280.1:n.*1250C=
ENST00000562308.5:c.104+14896C=
ENST00000565169.1:c.162+14896C=
ENST00000569170.5:c.162+14896C=
NM_001195794.1:c.*1250C= , LRG_700t1:c.*1250C=	NP_001182723.1:n.*1250C=
NM_001256819.1:c.*1563C=	NP_001243748.1:n.*1563C=
NM_052995.2:c.*166C= , LRG_700t2:c.*166C=	NP_443721.1:n.*166C=
NM_174878.2:c.*1250C=	NP_777367.1:n.*1250C=
NR_046380.2:n.2430C=
XR_924167.1:n.2261C=
NM_001256819.2:c.*1563C=	NP_001243748.1:n.*1563C=
NM_174878.3:c.*1250C= MANE Select	NP_777367.1:n.*1250C=
NR_046380.3:n.2158C=