Canonical Allele Identifier: CA2758898279

Gene: CLRN1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.150940676_150940677insACA , CM000665.2:g.150940676_150940677insACA	GRCh38
NC_000003.11:g.150658463_150658464insACA , CM000665.1:g.150658463_150658464insACA	GRCh37
NC_000003.10:g.152141153_152141154insACA	NCBI36
NG_009168.1:g.37323_37324insTGT , LRG_700:g.37323_37324insTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327047.6:c.433+905_433+906insTGT MANE Select	ENSP00000322280.1:n.433+905_433+906insTGT
ENST00000468836.2:c.581+905_581+906insTGT	ENSP00000419892.2:n.581+905_581+906insTGT
ENST00000644099.1:c.426-158_426-157insTGT	ENSP00000494762.1:n.426-158_426-157insTGT
ENST00000295911.6:c.205+905_205+906insTGT	ENSP00000295911.2:n.205+905_205+906insTGT
ENST00000327047.5:c.433+905_433+906insTGT	ENSP00000322280.1:n.433+905_433+906insTGT
ENST00000328863.8:c.434-158_434-157insTGT	ENSP00000329158.4:n.434-158_434-157insTGT
ENST00000468836.1:c.205+905_205+906insTGT	ENSP00000419892.1:n.205+905_205+906insTGT
ENST00000485607.1:c.97+905_97+906insTGT	ENSP00000419244.1:n.97+905_97+906insTGT
ENST00000562308.5:c.104+905_104+906insTGT
ENST00000565169.1:c.162+905_162+906insTGT
ENST00000569170.5:c.162+905_162+906insTGT
NM_001195794.1:c.434-158_434-157insTGT , LRG_700t1:c.434-158_434-157insTGT	NP_001182723.1:n.434-158_434-157insTGT
NM_001256819.1:c.*47+905_*47+906insTGT	NP_001243748.1:n.*47+905_*47+906insTGT
NM_052995.2:c.205+905_205+906insTGT , LRG_700t2:c.205+905_205+906insTGT	NP_443721.1:n.205+905_205+906insTGT
NM_174878.2:c.433+905_433+906insTGT	NP_777367.1:n.433+905_433+906insTGT
NR_046380.2:n.876-158_876-157insTGT
XR_924167.1:n.745+905_745+906insTGT
NM_001256819.2:c.*47+905_*47+906insTGT	NP_001243748.1:n.*47+905_*47+906insTGT
NM_174878.3:c.433+905_433+906insTGT MANE Select	NP_777367.1:n.433+905_433+906insTGT
NR_046380.3:n.604-158_604-157insTGT