Canonical Allele Identifier: CA1410882636

Gene: CLRN1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.150926747C= , CM000665.2:g.150926747C=	GRCh38
NC_000003.11:g.150644534C= , CM000665.1:g.150644534C=	GRCh37
NC_000003.10:g.152127224C=	NCBI36
NG_009168.1:g.51253G= , LRG_700:g.51253G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327047.6:c.*1189G= MANE Select	ENSP00000322280.1:n.*1189G=
ENST00000295911.6:c.*105G=	ENSP00000295911.2:n.*105G=
ENST00000327047.5:c.*1189G=	ENSP00000322280.1:n.*1189G=
ENST00000562308.5:c.104+14835G=
ENST00000565169.1:c.162+14835G=
ENST00000569170.5:c.162+14835G=
NM_001195794.1:c.*1189G= , LRG_700t1:c.*1189G=	NP_001182723.1:n.*1189G=
NM_001256819.1:c.*1502G=	NP_001243748.1:n.*1502G=
NM_052995.2:c.*105G= , LRG_700t2:c.*105G=	NP_443721.1:n.*105G=
NM_174878.2:c.*1189G=	NP_777367.1:n.*1189G=
NR_046380.2:n.2369G=
XR_924167.1:n.2200G=
NM_001256819.2:c.*1502G=	NP_001243748.1:n.*1502G=
NM_174878.3:c.*1189G= MANE Select	NP_777367.1:n.*1189G=
NR_046380.3:n.2097G=