Canonical Allele Identifier: CA900632826

Gene: CLRN1

Linked Data

• dbSNP Id: rs1254006815
• gnomAD v3: 3-150940430-TG-T
• gnomAD v4: 3-150940430-TG-T
• MyVariant Identifiers: chr3:g.150658218del (hg19) ; chr3:g.150940431del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.150940434del , CM000665.2:g.150940434del	GRCh38
NC_000003.11:g.150658221del , CM000665.1:g.150658221del	GRCh37
NC_000003.10:g.152140911del	NCBI36
NG_009168.1:g.37569del , LRG_700:g.37569del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327047.6:c.433+1151del MANE Select	ENSP00000322280.1:n.433+1151del
ENST00000468836.2:c.581+1151del	ENSP00000419892.2:n.581+1151del
ENST00000295911.6:c.205+1151del	ENSP00000295911.2:n.205+1151del
ENST00000327047.5:c.433+1151del	ENSP00000322280.1:n.433+1151del
ENST00000328863.8:c.472+50del	ENSP00000329158.4:n.472+50del
ENST00000468836.1:c.205+1151del	ENSP00000419892.1:n.205+1151del
ENST00000485607.1:c.97+1151del	ENSP00000419244.1:n.97+1151del
ENST00000562308.5:c.104+1151del
ENST00000565169.1:c.162+1151del
ENST00000569170.5:c.162+1151del
NM_001195794.1:c.472+50del , LRG_700t1:c.472+50del	NP_001182723.1:n.472+50del
NM_001256819.1:c.*47+1151del	NP_001243748.1:n.*47+1151del
NM_052995.2:c.205+1151del , LRG_700t2:c.205+1151del	NP_443721.1:n.205+1151del
NM_174878.2:c.433+1151del	NP_777367.1:n.433+1151del
NR_046380.2:n.914+50del
XR_924167.1:n.745+1151del
NM_001256819.2:c.*47+1151del	NP_001243748.1:n.*47+1151del
NM_174878.3:c.433+1151del MANE Select	NP_777367.1:n.433+1151del
NR_046380.3:n.642+50del