Canonical Allele Identifier: CA2758898226

Gene: CLRN1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.150940413_150940414del , CM000665.2:g.150940413_150940414del	GRCh38
NC_000003.11:g.150658200_150658201del , CM000665.1:g.150658200_150658201del	GRCh37
NC_000003.10:g.152140890_152140891del	NCBI36
NG_009168.1:g.37587_37588del , LRG_700:g.37587_37588del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327047.6:c.433+1169_433+1170del MANE Select	ENSP00000322280.1:n.433+1169_433+1170del
ENST00000468836.2:c.581+1169_581+1170del	ENSP00000419892.2:n.581+1169_581+1170del
ENST00000295911.6:c.205+1169_205+1170del	ENSP00000295911.2:n.205+1169_205+1170del
ENST00000327047.5:c.433+1169_433+1170del	ENSP00000322280.1:n.433+1169_433+1170del
ENST00000328863.8:c.472+68_472+69del	ENSP00000329158.4:n.472+68_472+69del
ENST00000468836.1:c.205+1169_205+1170del	ENSP00000419892.1:n.205+1169_205+1170del
ENST00000485607.1:c.97+1169_97+1170del	ENSP00000419244.1:n.97+1169_97+1170del
ENST00000562308.5:c.104+1169_104+1170del
ENST00000565169.1:c.162+1169_162+1170del
ENST00000569170.5:c.162+1169_162+1170del
NM_001195794.1:c.472+68_472+69del , LRG_700t1:c.472+68_472+69del	NP_001182723.1:n.472+68_472+69del
NM_001256819.1:c.*47+1169_*47+1170del	NP_001243748.1:n.*47+1169_*47+1170del
NM_052995.2:c.205+1169_205+1170del , LRG_700t2:c.205+1169_205+1170del	NP_443721.1:n.205+1169_205+1170del
NM_174878.2:c.433+1169_433+1170del	NP_777367.1:n.433+1169_433+1170del
NR_046380.2:n.914+68_914+69del
XR_924167.1:n.745+1169_745+1170del
NM_001256819.2:c.*47+1169_*47+1170del	NP_001243748.1:n.*47+1169_*47+1170del
NM_174878.3:c.433+1169_433+1170del MANE Select	NP_777367.1:n.433+1169_433+1170del
NR_046380.3:n.642+68_642+69del