Canonical Allele Identifier: CA355012328

Gene: CLRN1 CLRN1-AS1

Linked Data

• MyVariant Identifiers: chr3:g.150690495T>G (hg19) ; chr3:g.150972708T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.150972708T>G , CM000665.2:g.150972708T>G	GRCh38
NC_000003.11:g.150690495T>G , CM000665.1:g.150690495T>G	GRCh37
NC_000003.10:g.152173185T>G	NCBI36
NG_009168.1:g.5292A>C , LRG_700:g.5292A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000327047.6:c.1A>C (CLRN1) MANE Select	ENSP00000322280.1:p.Met1Leu
ENST00000327047.5:c.1A>C (CLRN1)	ENSP00000322280.1:p.Met1Leu
ENST00000328863.8:c.1A>C (CLRN1)	ENSP00000329158.4:p.Met1Leu
ENST00000472224.1:n.7A>C (CLRN1)
NM_001195794.1:c.1A>C , LRG_700t1:c.1A>C (CLRN1)	NP_001182723.1:p.Met1Leu
NM_001256819.1:c.1A>C (CLRN1)	NP_001243748.1:p.Met1Leu
NM_174878.2:c.1A>C (CLRN1)	NP_777367.1:p.Met1Leu
NR_024066.1:n.31T>G (CLRN1-AS1)
NR_046380.2:n.292A>C (CLRN1)
XR_924167.1:n.313A>C (CLRN1)
NR_024066.2:n.31T>G (CLRN1-AS1)
NM_001256819.2:c.1A>C (CLRN1)	NP_001243748.1:p.Met1Leu
NM_174878.3:c.1A>C (CLRN1) MANE Select	NP_777367.1:p.Met1Leu
NR_046380.3:n.20A>C (CLRN1)