Canonical Allele Identifier: CA1410887977

Gene: CLRN1

Linked Data

• dbSNP Id: rs1713768150

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.150940703_150940706del , CM000665.2:g.150940703_150940706del	GRCh38
NC_000003.11:g.150658490_150658493del , CM000665.1:g.150658490_150658493del	GRCh37
NC_000003.10:g.152141180_152141183del	NCBI36
NG_009168.1:g.37294_37297del , LRG_700:g.37294_37297del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327047.6:c.433+876_433+879del MANE Select	ENSP00000322280.1:n.433+876_433+879del
ENST00000468836.2:c.581+876_581+879del	ENSP00000419892.2:n.581+876_581+879del
ENST00000644099.1:c.426-187_426-184del	ENSP00000494762.1:n.426-187_426-184del
ENST00000295911.6:c.205+876_205+879del	ENSP00000295911.2:n.205+876_205+879del
ENST00000327047.5:c.433+876_433+879del	ENSP00000322280.1:n.433+876_433+879del
ENST00000328863.8:c.434-187_434-184del	ENSP00000329158.4:n.434-187_434-184del
ENST00000468836.1:c.205+876_205+879del	ENSP00000419892.1:n.205+876_205+879del
ENST00000485607.1:c.97+876_97+879del	ENSP00000419244.1:n.97+876_97+879del
ENST00000562308.5:c.104+876_104+879del
ENST00000565169.1:c.162+876_162+879del
ENST00000569170.5:c.162+876_162+879del
NM_001195794.1:c.434-187_434-184del , LRG_700t1:c.434-187_434-184del	NP_001182723.1:n.434-187_434-184del
NM_001256819.1:c.*47+876_*47+879del	NP_001243748.1:n.*47+876_*47+879del
NM_052995.2:c.205+876_205+879del , LRG_700t2:c.205+876_205+879del	NP_443721.1:n.205+876_205+879del
NM_174878.2:c.433+876_433+879del	NP_777367.1:n.433+876_433+879del
NR_046380.2:n.876-187_876-184del
XR_924167.1:n.745+876_745+879del
NM_001256819.2:c.*47+876_*47+879del	NP_001243748.1:n.*47+876_*47+879del
NM_174878.3:c.433+876_433+879del MANE Select	NP_777367.1:n.433+876_433+879del
NR_046380.3:n.604-187_604-184del