Canonical Allele Identifier: CA1410882657

Gene: CLRN1

Linked Data

• dbSNP Id: rs1319828358
• gnomAD v4: 3-150926790-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.150926790T>C , CM000665.2:g.150926790T>C	GRCh38
NC_000003.11:g.150644577T>C , CM000665.1:g.150644577T>C	GRCh37
NC_000003.10:g.152127267T>C	NCBI36
NG_009168.1:g.51210A>G , LRG_700:g.51210A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000327047.6:c.*1146A>G MANE Select	ENSP00000322280.1:n.*1146A>G
ENST00000295911.6:c.*62A>G	ENSP00000295911.2:n.*62A>G
ENST00000327047.5:c.*1146A>G	ENSP00000322280.1:n.*1146A>G
ENST00000562308.5:c.104+14792A>G
ENST00000565169.1:c.162+14792A>G
ENST00000569170.5:c.162+14792A>G
NM_001195794.1:c.*1146A>G , LRG_700t1:c.*1146A>G	NP_001182723.1:n.*1146A>G
NM_001256819.1:c.*1459A>G	NP_001243748.1:n.*1459A>G
NM_052995.2:c.*62A>G , LRG_700t2:c.*62A>G	NP_443721.1:n.*62A>G
NM_174878.2:c.*1146A>G	NP_777367.1:n.*1146A>G
NR_046380.2:n.2326A>G
XR_924167.1:n.2157A>G
NM_001256819.2:c.*1459A>G	NP_001243748.1:n.*1459A>G
NM_174878.3:c.*1146A>G MANE Select	NP_777367.1:n.*1146A>G
NR_046380.3:n.2054A>G