Canonical Allele Identifier: CA1410883272

Gene: CLRN1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.150928184C= , CM000665.2:g.150928184C=	GRCh38
NC_000003.11:g.150645971C= , CM000665.1:g.150645971C=	GRCh37
NC_000003.10:g.152128661C=	NCBI36
NG_009168.1:g.49816G= , LRG_700:g.49816G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327047.6:c.451G= MANE Select	ENSP00000322280.1:p.Val151=
ENST00000468836.2:c.599G=	ENSP00000419892.2:n.599G=
ENST00000295911.6:c.223G=	ENSP00000295911.2:p.Val75=
ENST00000327047.5:c.451G=	ENSP00000322280.1:p.Val151=
ENST00000328863.8:c.490G=	ENSP00000329158.4:p.Val164=
ENST00000468836.1:c.223G=	ENSP00000419892.1:p.Val75=
ENST00000485607.1:c.115G=	ENSP00000419244.1:p.Val39=
ENST00000562308.5:c.104+13398G=
ENST00000565169.1:c.162+13398G=
ENST00000569170.5:c.162+13398G=
NM_001195794.1:c.490G= , LRG_700t1:c.490G=	NP_001182723.1:p.Val164=
NM_001256819.1:c.*65G=	NP_001243748.1:n.*65G=
NM_052995.2:c.223G= , LRG_700t2:c.223G=	NP_443721.1:p.Val75=
NM_174878.2:c.451G=	NP_777367.1:p.Val151=
NR_046380.2:n.932G=
XR_924167.1:n.763G=
NM_001256819.2:c.*65G=	NP_001243748.1:n.*65G=
NM_174878.3:c.451G= MANE Select	NP_777367.1:p.Val151=
NR_046380.3:n.660G=