Canonical Allele Identifier: CA1410888628

Gene: CLRN1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.150941920_150941921delinsAG , CM000665.2:g.150941920_150941921delinsAG	GRCh38
NC_000003.11:g.150659707_150659708delinsAG , CM000665.1:g.150659707_150659708delinsAG	GRCh37
NC_000003.10:g.152142397_152142398delinsAG	NCBI36
NG_009168.1:g.36079_36080delinsCT , LRG_700:g.36079_36080delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327047.6:c.254-160_254-159delinsCT MANE Select	ENSP00000322280.1:n.254-160_254-159delinsCT
ENST00000468836.2:c.402-160_402-159delinsCT	ENSP00000419892.2:n.402-160_402-159delinsCT
ENST00000644099.1:c.246-160_246-159delinsCT	ENSP00000494762.1:n.246-160_246-159delinsCT
ENST00000295911.6:c.26-160_26-159delinsCT	ENSP00000295911.2:n.26-160_26-159delinsCT
ENST00000327047.5:c.254-160_254-159delinsCT	ENSP00000322280.1:n.254-160_254-159delinsCT
ENST00000328863.8:c.254-160_254-159delinsCT	ENSP00000329158.4:n.254-160_254-159delinsCT
ENST00000468836.1:c.26-160_26-159delinsCT	ENSP00000419892.1:n.26-160_26-159delinsCT
ENST00000472224.1:n.260-160_260-159delinsCT
ENST00000485607.1:c.-83-160_-83-159delinsCT	ENSP00000419244.1:n.-83-160_-83-159delinsCT
NM_001195794.1:c.254-160_254-159delinsCT , LRG_700t1:c.254-160_254-159delinsCT	NP_001182723.1:n.254-160_254-159delinsCT
NM_001256819.1:c.426-160_426-159delinsCT	NP_001243748.1:n.426-160_426-159delinsCT
NM_052995.2:c.26-160_26-159delinsCT , LRG_700t2:c.26-160_26-159delinsCT	NP_443721.1:n.26-160_26-159delinsCT
NM_174878.2:c.254-160_254-159delinsCT	NP_777367.1:n.254-160_254-159delinsCT
NR_046380.2:n.696-160_696-159delinsCT
XR_924167.1:n.566-160_566-159delinsCT
NM_001256819.2:c.426-160_426-159delinsCT	NP_001243748.1:n.426-160_426-159delinsCT
NM_174878.3:c.254-160_254-159delinsCT MANE Select	NP_777367.1:n.254-160_254-159delinsCT
NR_046380.3:n.424-160_424-159delinsCT