Canonical Allele Identifier: CA2668197889
Gene: CLRN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.150941907_150941913del , CM000665.2:g.150941907_150941913del GRCh38
NC_000003.11:g.150659694_150659700del , CM000665.1:g.150659694_150659700del GRCh37
NC_000003.10:g.152142384_152142390del NCBI36
NG_009168.1:g.36087_36093del , LRG_700:g.36087_36093del

Transcript Alleles

HGVS Amino-acid Change
ENST00000327047.6:c.254-152_254-146del MANE Select ENSP00000322280.1:n.254-152_254-146del
ENST00000468836.2:c.402-152_402-146del ENSP00000419892.2:n.402-152_402-146del
ENST00000644099.1:c.246-152_246-146del ENSP00000494762.1:n.246-152_246-146del
ENST00000295911.6:c.26-152_26-146del ENSP00000295911.2:n.26-152_26-146del
ENST00000327047.5:c.254-152_254-146del ENSP00000322280.1:n.254-152_254-146del
ENST00000328863.8:c.254-152_254-146del ENSP00000329158.4:n.254-152_254-146del
ENST00000468836.1:c.26-152_26-146del ENSP00000419892.1:n.26-152_26-146del
ENST00000472224.1:n.260-152_260-146del
ENST00000485607.1:c.-83-152_-83-146del ENSP00000419244.1:n.-83-152_-83-146del
NM_001195794.1:c.254-152_254-146del , LRG_700t1:c.254-152_254-146del NP_001182723.1:n.254-152_254-146del
NM_001256819.1:c.426-152_426-146del NP_001243748.1:n.426-152_426-146del
NM_052995.2:c.26-152_26-146del , LRG_700t2:c.26-152_26-146del NP_443721.1:n.26-152_26-146del
NM_174878.2:c.254-152_254-146del NP_777367.1:n.254-152_254-146del
NR_046380.2:n.696-152_696-146del
XR_924167.1:n.566-152_566-146del
NM_001256819.2:c.426-152_426-146del NP_001243748.1:n.426-152_426-146del
NM_174878.3:c.254-152_254-146del MANE Select NP_777367.1:n.254-152_254-146del
NR_046380.3:n.424-152_424-146del