Canonical Allele Identifier: CA1410882525
Gene: CLRN1 HGNC NCBI

Linked Data

dbSNP Id: rs1712799206

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.150926518G>C , CM000665.2:g.150926518G>C GRCh38
NC_000003.11:g.150644305G>C , CM000665.1:g.150644305G>C GRCh37
NC_000003.10:g.152126995G>C NCBI36
NG_009168.1:g.51482C>G , LRG_700:g.51482C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000295911.6:c.*334C>G ENSP00000295911.2:n.*334C>G
ENST00000562308.5:c.104+15064C>G
ENST00000565169.1:c.162+15064C>G
ENST00000569170.5:c.162+15064C>G
NM_052995.2:c.*334C>G , LRG_700t2:c.*334C>G NP_443721.1:n.*334C>G
XR_924167.1:n.2429C>G