Canonical Allele Identifier: CA900633103

Gene: CLRN1

Linked Data

• dbSNP Id: rs1369116739
• MyVariant Identifiers: chr3:g.150658599del (hg19) ; chr3:g.150940812del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.150940813del , CM000665.2:g.150940813del	GRCh38
NC_000003.11:g.150658600del , CM000665.1:g.150658600del	GRCh37
NC_000003.10:g.152141290del	NCBI36
NG_009168.1:g.37188del , LRG_700:g.37188del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327047.6:c.433+770del MANE Select	ENSP00000322280.1:n.433+770del
ENST00000468836.2:c.581+770del	ENSP00000419892.2:n.581+770del
ENST00000644099.1:c.426-293del	ENSP00000494762.1:n.426-293del
ENST00000295911.6:c.205+770del	ENSP00000295911.2:n.205+770del
ENST00000327047.5:c.433+770del	ENSP00000322280.1:n.433+770del
ENST00000328863.8:c.434-293del	ENSP00000329158.4:n.434-293del
ENST00000468836.1:c.205+770del	ENSP00000419892.1:n.205+770del
ENST00000485607.1:c.97+770del	ENSP00000419244.1:n.97+770del
ENST00000562308.5:c.104+770del
ENST00000565169.1:c.162+770del
ENST00000569170.5:c.162+770del
NM_001195794.1:c.434-293del , LRG_700t1:c.434-293del	NP_001182723.1:n.434-293del
NM_001256819.1:c.*47+770del	NP_001243748.1:n.*47+770del
NM_052995.2:c.205+770del , LRG_700t2:c.205+770del	NP_443721.1:n.205+770del
NM_174878.2:c.433+770del	NP_777367.1:n.433+770del
NR_046380.2:n.876-293del
XR_924167.1:n.745+770del
NM_001256819.2:c.*47+770del	NP_001243748.1:n.*47+770del
NM_174878.3:c.433+770del MANE Select	NP_777367.1:n.433+770del
NR_046380.3:n.604-293del