Canonical Allele Identifier: CA1410883188

Gene: CLRN1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.150927965T= , CM000665.2:g.150927965T=	GRCh38
NC_000003.11:g.150645752T= , CM000665.1:g.150645752T=	GRCh37
NC_000003.10:g.152128442T=	NCBI36
NG_009168.1:g.50035A= , LRG_700:g.50035A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327047.6:c.670A= MANE Select	ENSP00000322280.1:p.Thr224=
ENST00000295911.6:c.342+100A=	ENSP00000295911.2:n.342+100A=
ENST00000327047.5:c.670A=	ENSP00000322280.1:p.Thr224=
ENST00000328863.8:c.709A=	ENSP00000329158.4:p.Thr237=
ENST00000562308.5:c.104+13617A=
ENST00000565169.1:c.162+13617A=
ENST00000569170.5:c.162+13617A=
NM_001195794.1:c.709A= , LRG_700t1:c.709A=	NP_001182723.1:p.Thr237=
NM_001256819.1:c.*284A=	NP_001243748.1:n.*284A=
NM_052995.2:c.342+100A= , LRG_700t2:c.342+100A=	NP_443721.1:n.342+100A=
NM_174878.2:c.670A=	NP_777367.1:p.Thr224=
NR_046380.2:n.1151A=
XR_924167.1:n.982A=
NM_001256819.2:c.*284A=	NP_001243748.1:n.*284A=
NM_174878.3:c.670A= MANE Select	NP_777367.1:p.Thr224=
NR_046380.3:n.879A=