Canonical Allele Identifier: CA1410882532
Gene: CLRN1 HGNC NCBI

Linked Data

dbSNP Id: rs1024943527
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.150926536A>G , CM000665.2:g.150926536A>G GRCh38
NC_000003.11:g.150644323A>G , CM000665.1:g.150644323A>G GRCh37
NC_000003.10:g.152127013A>G NCBI36
NG_009168.1:g.51464T>C , LRG_700:g.51464T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000295911.6:c.*316T>C ENSP00000295911.2:n.*316T>C
ENST00000562308.5:c.104+15046T>C
ENST00000565169.1:c.162+15046T>C
ENST00000569170.5:c.162+15046T>C
NM_052995.2:c.*316T>C , LRG_700t2:c.*316T>C NP_443721.1:n.*316T>C
XR_924167.1:n.2411T>C
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