Canonical Allele Identifier: CA354953460

Gene: CLRN1

Linked Data

• dbSNP Id: rs1576623537
• MyVariant Identifiers: chr3:g.150645975A>C (hg19) ; chr3:g.150928188A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.150928188A>C , CM000665.2:g.150928188A>C	GRCh38
NC_000003.11:g.150645975A>C , CM000665.1:g.150645975A>C	GRCh37
NC_000003.10:g.152128665A>C	NCBI36
NG_009168.1:g.49812T>G , LRG_700:g.49812T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327047.6:c.447T>G MANE Select	ENSP00000322280.1:p.Cys149Trp
ENST00000468836.2:c.595T>G	ENSP00000419892.2:n.595T>G
ENST00000295911.6:c.219T>G	ENSP00000295911.2:p.Cys73Trp
ENST00000327047.5:c.447T>G	ENSP00000322280.1:p.Cys149Trp
ENST00000328863.8:c.486T>G	ENSP00000329158.4:p.Cys162Trp
ENST00000468836.1:c.219T>G	ENSP00000419892.1:p.Cys73Trp
ENST00000485607.1:c.111T>G	ENSP00000419244.1:p.Cys37Trp
ENST00000562308.5:c.104+13394T>G
ENST00000565169.1:c.162+13394T>G
ENST00000569170.5:c.162+13394T>G
NM_001195794.1:c.486T>G , LRG_700t1:c.486T>G	NP_001182723.1:p.Cys162Trp
NM_001256819.1:c.*61T>G	NP_001243748.1:n.*61T>G
NM_052995.2:c.219T>G , LRG_700t2:c.219T>G	NP_443721.1:p.Cys73Trp
NM_174878.2:c.447T>G	NP_777367.1:p.Cys149Trp
NR_046380.2:n.928T>G
XR_924167.1:n.759T>G
NM_001256819.2:c.*61T>G	NP_001243748.1:n.*61T>G
NM_174878.3:c.447T>G MANE Select	NP_777367.1:p.Cys149Trp
NR_046380.3:n.656T>G