Canonical Allele Identifier: CA85691925
Gene: CLRN1 HGNC NCBI

Linked Data

dbSNP Id: rs113261575

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.150941972_150941973del , CM000665.2:g.150941972_150941973del GRCh38
NC_000003.11:g.150659759_150659760del , CM000665.1:g.150659759_150659760del GRCh37
NC_000003.10:g.152142449_152142450del NCBI36
NG_009168.1:g.36029_36030del , LRG_700:g.36029_36030del

Transcript Alleles

HGVS Amino-acid Change
ENST00000327047.6:c.254-210_254-209del MANE Select ENSP00000322280.1:n.254-210_254-209del
ENST00000468836.2:c.402-210_402-209del ENSP00000419892.2:n.402-210_402-209del
ENST00000644099.1:c.246-210_246-209del ENSP00000494762.1:n.246-210_246-209del
ENST00000295911.6:c.26-210_26-209del ENSP00000295911.2:n.26-210_26-209del
ENST00000327047.5:c.254-210_254-209del ENSP00000322280.1:n.254-210_254-209del
ENST00000328863.8:c.254-210_254-209del ENSP00000329158.4:n.254-210_254-209del
ENST00000468836.1:c.26-210_26-209del ENSP00000419892.1:n.26-210_26-209del
ENST00000472224.1:n.260-210_260-209del
ENST00000485607.1:c.-83-210_-83-209del ENSP00000419244.1:n.-83-210_-83-209del
NM_001195794.1:c.254-210_254-209del , LRG_700t1:c.254-210_254-209del NP_001182723.1:n.254-210_254-209del
NM_001256819.1:c.426-210_426-209del NP_001243748.1:n.426-210_426-209del
NM_052995.2:c.26-210_26-209del , LRG_700t2:c.26-210_26-209del NP_443721.1:n.26-210_26-209del
NM_174878.2:c.254-210_254-209del NP_777367.1:n.254-210_254-209del
NR_046380.2:n.696-210_696-209del
XR_924167.1:n.566-210_566-209del
NM_001256819.2:c.426-210_426-209del NP_001243748.1:n.426-210_426-209del
NM_174878.3:c.254-210_254-209del MANE Select NP_777367.1:n.254-210_254-209del
NR_046380.3:n.424-210_424-209del