Canonical Allele Identifier: CA355012283

Gene: CLRN1 CLRN1-AS1

Linked Data

• MyVariant Identifiers: chr3:g.150690484T>G (hg19) ; chr3:g.150972697T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.150972697T>G , CM000665.2:g.150972697T>G	GRCh38
NC_000003.11:g.150690484T>G , CM000665.1:g.150690484T>G	GRCh37
NC_000003.10:g.152173174T>G	NCBI36
NG_009168.1:g.5303A>C , LRG_700:g.5303A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327047.6:c.12A>C (CLRN1) MANE Select	ENSP00000322280.1:p.Gln4His
ENST00000327047.5:c.12A>C (CLRN1)	ENSP00000322280.1:p.Gln4His
ENST00000328863.8:c.12A>C (CLRN1)	ENSP00000329158.4:p.Gln4His
ENST00000472224.1:n.18A>C (CLRN1)
NM_001195794.1:c.12A>C , LRG_700t1:c.12A>C (CLRN1)	NP_001182723.1:p.Gln4His
NM_001256819.1:c.12A>C (CLRN1)	NP_001243748.1:p.Gln4His
NM_174878.2:c.12A>C (CLRN1)	NP_777367.1:p.Gln4His
NR_024066.1:n.20T>G (CLRN1-AS1)
NR_046380.2:n.303A>C (CLRN1)
XR_924167.1:n.324A>C (CLRN1)
NR_024066.2:n.20T>G (CLRN1-AS1)
NM_001256819.2:c.12A>C (CLRN1)	NP_001243748.1:p.Gln4His
NM_174878.3:c.12A>C (CLRN1) MANE Select	NP_777367.1:p.Gln4His
NR_046380.3:n.31A>C (CLRN1)