Canonical Allele Identifier: CA355012327

Gene: CLRN1 CLRN1-AS1

Linked Data

• MyVariant Identifiers: chr3:g.150690494A>T (hg19) ; chr3:g.150972707A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.150972707A>T , CM000665.2:g.150972707A>T	GRCh38
NC_000003.11:g.150690494A>T , CM000665.1:g.150690494A>T	GRCh37
NC_000003.10:g.152173184A>T	NCBI36
NG_009168.1:g.5293T>A , LRG_700:g.5293T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327047.6:c.2T>A (CLRN1) MANE Select	ENSP00000322280.1:p.Met1Lys
ENST00000327047.5:c.2T>A (CLRN1)	ENSP00000322280.1:p.Met1Lys
ENST00000328863.8:c.2T>A (CLRN1)	ENSP00000329158.4:p.Met1Lys
ENST00000472224.1:n.8T>A (CLRN1)
NM_001195794.1:c.2T>A , LRG_700t1:c.2T>A (CLRN1)	NP_001182723.1:p.Met1Lys
NM_001256819.1:c.2T>A (CLRN1)	NP_001243748.1:p.Met1Lys
NM_174878.2:c.2T>A (CLRN1)	NP_777367.1:p.Met1Lys
NR_024066.1:n.30A>T (CLRN1-AS1)
NR_046380.2:n.293T>A (CLRN1)
XR_924167.1:n.314T>A (CLRN1)
NR_024066.2:n.30A>T (CLRN1-AS1)
NM_001256819.2:c.2T>A (CLRN1)	NP_001243748.1:p.Met1Lys
NM_174878.3:c.2T>A (CLRN1) MANE Select	NP_777367.1:p.Met1Lys
NR_046380.3:n.21T>A (CLRN1)