Canonical Allele Identifier: CA1410888018

Gene: CLRN1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.150940811_150940812delinsTC , CM000665.2:g.150940811_150940812delinsTC	GRCh38
NC_000003.11:g.150658598_150658599delinsTC , CM000665.1:g.150658598_150658599delinsTC	GRCh37
NC_000003.10:g.152141288_152141289delinsTC	NCBI36
NG_009168.1:g.37188_37189delinsGA , LRG_700:g.37188_37189delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327047.6:c.433+770_433+771delinsGA MANE Select	ENSP00000322280.1:n.433+770_433+771delinsGA
ENST00000468836.2:c.581+770_581+771delinsGA	ENSP00000419892.2:n.581+770_581+771delinsGA
ENST00000644099.1:c.426-293_426-292delinsGA	ENSP00000494762.1:n.426-293_426-292delinsGA
ENST00000295911.6:c.205+770_205+771delinsGA	ENSP00000295911.2:n.205+770_205+771delinsGA
ENST00000327047.5:c.433+770_433+771delinsGA	ENSP00000322280.1:n.433+770_433+771delinsGA
ENST00000328863.8:c.434-293_434-292delinsGA	ENSP00000329158.4:n.434-293_434-292delinsGA
ENST00000468836.1:c.205+770_205+771delinsGA	ENSP00000419892.1:n.205+770_205+771delinsGA
ENST00000485607.1:c.97+770_97+771delinsGA	ENSP00000419244.1:n.97+770_97+771delinsGA
ENST00000562308.5:c.104+770_104+771delinsGA
ENST00000565169.1:c.162+770_162+771delinsGA
ENST00000569170.5:c.162+770_162+771delinsGA
NM_001195794.1:c.434-293_434-292delinsGA , LRG_700t1:c.434-293_434-292delinsGA	NP_001182723.1:n.434-293_434-292delinsGA
NM_001256819.1:c.*47+770_*47+771delinsGA	NP_001243748.1:n.*47+770_*47+771delinsGA
NM_052995.2:c.205+770_205+771delinsGA , LRG_700t2:c.205+770_205+771delinsGA	NP_443721.1:n.205+770_205+771delinsGA
NM_174878.2:c.433+770_433+771delinsGA	NP_777367.1:n.433+770_433+771delinsGA
NR_046380.2:n.876-293_876-292delinsGA
XR_924167.1:n.745+770_745+771delinsGA
NM_001256819.2:c.*47+770_*47+771delinsGA	NP_001243748.1:n.*47+770_*47+771delinsGA
NM_174878.3:c.433+770_433+771delinsGA MANE Select	NP_777367.1:n.433+770_433+771delinsGA
NR_046380.3:n.604-293_604-292delinsGA