Canonical Allele Identifier: CA1410882468
Gene: CLRN1 HGNC NCBI

Linked Data

dbSNP Id: rs1712792788

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.150926393T>C , CM000665.2:g.150926393T>C GRCh38
NC_000003.11:g.150644180T>C , CM000665.1:g.150644180T>C GRCh37
NC_000003.10:g.152126870T>C NCBI36
NG_009168.1:g.51607A>G , LRG_700:g.51607A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000295911.6:c.*459A>G ENSP00000295911.2:n.*459A>G
ENST00000562308.5:c.104+15189A>G
ENST00000565169.1:c.162+15189A>G
ENST00000569170.5:c.162+15189A>G
NM_052995.2:c.*459A>G , LRG_700t2:c.*459A>G NP_443721.1:n.*459A>G
XR_924167.1:n.2554A>G