Canonical Allele Identifier: CA1410882942

Gene: CLRN1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.150927474A= , CM000665.2:g.150927474A=	GRCh38
NC_000003.11:g.150645261A= , CM000665.1:g.150645261A=	GRCh37
NC_000003.10:g.152127951A=	NCBI36
NG_009168.1:g.50526T= , LRG_700:g.50526T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000327047.6:c.*462T= MANE Select	ENSP00000322280.1:n.*462T=
ENST00000295911.6:c.342+591T=	ENSP00000295911.2:n.342+591T=
ENST00000327047.5:c.*462T=	ENSP00000322280.1:n.*462T=
ENST00000562308.5:c.104+14108T=
ENST00000565169.1:c.162+14108T=
ENST00000569170.5:c.162+14108T=
NM_001195794.1:c.*462T= , LRG_700t1:c.*462T=	NP_001182723.1:n.*462T=
NM_001256819.1:c.*775T=	NP_001243748.1:n.*775T=
NM_052995.2:c.342+591T= , LRG_700t2:c.342+591T=	NP_443721.1:n.342+591T=
NM_174878.2:c.*462T=	NP_777367.1:n.*462T=
NR_046380.2:n.1642T=
XR_924167.1:n.1473T=
NM_001256819.2:c.*775T=	NP_001243748.1:n.*775T=
NM_174878.3:c.*462T= MANE Select	NP_777367.1:n.*462T=
NR_046380.3:n.1370T=