Canonical Allele Identifier: CA1410882649

Gene: CLRN1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.150926778G= , CM000665.2:g.150926778G=	GRCh38
NC_000003.11:g.150644565G= , CM000665.1:g.150644565G=	GRCh37
NC_000003.10:g.152127255G=	NCBI36
NG_009168.1:g.51222C= , LRG_700:g.51222C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000327047.6:c.*1158C= MANE Select	ENSP00000322280.1:n.*1158C=
ENST00000295911.6:c.*74C=	ENSP00000295911.2:n.*74C=
ENST00000327047.5:c.*1158C=	ENSP00000322280.1:n.*1158C=
ENST00000562308.5:c.104+14804C=
ENST00000565169.1:c.162+14804C=
ENST00000569170.5:c.162+14804C=
NM_001195794.1:c.*1158C= , LRG_700t1:c.*1158C=	NP_001182723.1:n.*1158C=
NM_001256819.1:c.*1471C=	NP_001243748.1:n.*1471C=
NM_052995.2:c.*74C= , LRG_700t2:c.*74C=	NP_443721.1:n.*74C=
NM_174878.2:c.*1158C=	NP_777367.1:n.*1158C=
NR_046380.2:n.2338C=
XR_924167.1:n.2169C=
NM_001256819.2:c.*1471C=	NP_001243748.1:n.*1471C=
NM_174878.3:c.*1158C= MANE Select	NP_777367.1:n.*1158C=
NR_046380.3:n.2066C=