Canonical Allele Identifier: CA1410888010

Gene: CLRN1

Linked Data

• dbSNP Id: rs1713771912

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.150940794_150940813dup , CM000665.2:g.150940794_150940813dup	GRCh38
NC_000003.11:g.150658581_150658600dup , CM000665.1:g.150658581_150658600dup	GRCh37
NC_000003.10:g.152141271_152141290dup	NCBI36
NG_009168.1:g.37188_37207dup , LRG_700:g.37188_37207dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327047.6:c.433+770_433+789dup MANE Select	ENSP00000322280.1:n.433+770_433+789dup
ENST00000468836.2:c.581+770_581+789dup	ENSP00000419892.2:n.581+770_581+789dup
ENST00000644099.1:c.426-293_426-274dup	ENSP00000494762.1:n.426-293_426-274dup
ENST00000295911.6:c.205+770_205+789dup	ENSP00000295911.2:n.205+770_205+789dup
ENST00000327047.5:c.433+770_433+789dup	ENSP00000322280.1:n.433+770_433+789dup
ENST00000328863.8:c.434-293_434-274dup	ENSP00000329158.4:n.434-293_434-274dup
ENST00000468836.1:c.205+770_205+789dup	ENSP00000419892.1:n.205+770_205+789dup
ENST00000485607.1:c.97+770_97+789dup	ENSP00000419244.1:n.97+770_97+789dup
ENST00000562308.5:c.104+770_104+789dup
ENST00000565169.1:c.162+770_162+789dup
ENST00000569170.5:c.162+770_162+789dup
NM_001195794.1:c.434-293_434-274dup , LRG_700t1:c.434-293_434-274dup	NP_001182723.1:n.434-293_434-274dup
NM_001256819.1:c.*47+770_*47+789dup	NP_001243748.1:n.*47+770_*47+789dup
NM_052995.2:c.205+770_205+789dup , LRG_700t2:c.205+770_205+789dup	NP_443721.1:n.205+770_205+789dup
NM_174878.2:c.433+770_433+789dup	NP_777367.1:n.433+770_433+789dup
NR_046380.2:n.876-293_876-274dup
XR_924167.1:n.745+770_745+789dup
NM_001256819.2:c.*47+770_*47+789dup	NP_001243748.1:n.*47+770_*47+789dup
NM_174878.3:c.433+770_433+789dup MANE Select	NP_777367.1:n.433+770_433+789dup
NR_046380.3:n.604-293_604-274dup