Canonical Allele Identifier: CA2605478009
Gene: CLRN1 HGNC NCBI

Linked Data

dbSNP Id: rs2107951752

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.150941904_150941905del , CM000665.2:g.150941904_150941905del GRCh38
NC_000003.11:g.150659691_150659692del , CM000665.1:g.150659691_150659692del GRCh37
NC_000003.10:g.152142381_152142382del NCBI36
NG_009168.1:g.36097_36098del , LRG_700:g.36097_36098del

Transcript Alleles

HGVS Amino-acid Change
ENST00000327047.6:c.254-142_254-141del MANE Select ENSP00000322280.1:n.254-142_254-141del
ENST00000468836.2:c.402-142_402-141del ENSP00000419892.2:n.402-142_402-141del
ENST00000644099.1:c.246-142_246-141del ENSP00000494762.1:n.246-142_246-141del
ENST00000295911.6:c.26-142_26-141del ENSP00000295911.2:n.26-142_26-141del
ENST00000327047.5:c.254-142_254-141del ENSP00000322280.1:n.254-142_254-141del
ENST00000328863.8:c.254-142_254-141del ENSP00000329158.4:n.254-142_254-141del
ENST00000468836.1:c.26-142_26-141del ENSP00000419892.1:n.26-142_26-141del
ENST00000472224.1:n.260-142_260-141del
ENST00000485607.1:c.-83-142_-83-141del ENSP00000419244.1:n.-83-142_-83-141del
NM_001195794.1:c.254-142_254-141del , LRG_700t1:c.254-142_254-141del NP_001182723.1:n.254-142_254-141del
NM_001256819.1:c.426-142_426-141del NP_001243748.1:n.426-142_426-141del
NM_052995.2:c.26-142_26-141del , LRG_700t2:c.26-142_26-141del NP_443721.1:n.26-142_26-141del
NM_174878.2:c.254-142_254-141del NP_777367.1:n.254-142_254-141del
NR_046380.2:n.696-142_696-141del
XR_924167.1:n.566-142_566-141del
NM_001256819.2:c.426-142_426-141del NP_001243748.1:n.426-142_426-141del
NM_174878.3:c.254-142_254-141del MANE Select NP_777367.1:n.254-142_254-141del
NR_046380.3:n.424-142_424-141del