Canonical Allele Identifier: CA1410883127

Gene: CLRN1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.150927848C= , CM000665.2:g.150927848C=	GRCh38
NC_000003.11:g.150645635C= , CM000665.1:g.150645635C=	GRCh37
NC_000003.10:g.152128325C=	NCBI36
NG_009168.1:g.50152G= , LRG_700:g.50152G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000327047.6:c.*88G= MANE Select	ENSP00000322280.1:n.*88G=
ENST00000295911.6:c.342+217G=	ENSP00000295911.2:n.342+217G=
ENST00000327047.5:c.*88G=	ENSP00000322280.1:n.*88G=
ENST00000562308.5:c.104+13734G=
ENST00000565169.1:c.162+13734G=
ENST00000569170.5:c.162+13734G=
NM_001195794.1:c.*88G= , LRG_700t1:c.*88G=	NP_001182723.1:n.*88G=
NM_001256819.1:c.*401G=	NP_001243748.1:n.*401G=
NM_052995.2:c.342+217G= , LRG_700t2:c.342+217G=	NP_443721.1:n.342+217G=
NM_174878.2:c.*88G=	NP_777367.1:n.*88G=
NR_046380.2:n.1268G=
XR_924167.1:n.1099G=
NM_001256819.2:c.*401G=	NP_001243748.1:n.*401G=
NM_174878.3:c.*88G= MANE Select	NP_777367.1:n.*88G=
NR_046380.3:n.996G=