Canonical Allele Identifier: CA2666198
Gene: CLRN1 HGNC NCBI

Linked Data

dbSNP Id: rs182614686

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.150972544G>C , CM000665.2:g.150972544G>C GRCh38
NC_000003.11:g.150690331G>C , CM000665.1:g.150690331G>C GRCh37
NC_000003.10:g.152173021G>C NCBI36
NG_009168.1:g.5456C>G , LRG_700:g.5456C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000327047.6:c.165C>G MANE Select ENSP00000322280.1:p.Asp55Glu
ENST00000468836.2:c.141C>G ENSP00000419892.2:p.Asp47Glu
ENST00000644099.1:c.6C>G ENSP00000494762.1:p.Asp2Glu
ENST00000645441.1:c.7C>G
ENST00000327047.5:c.165C>G ENSP00000322280.1:p.Asp55Glu
ENST00000328863.8:c.165C>G ENSP00000329158.4:p.Asp55Glu
ENST00000468836.1:c.-236C>G ENSP00000419892.1:n.-236C>G
ENST00000472224.1:n.171C>G
NM_001195794.1:c.165C>G , LRG_700t1:c.165C>G NP_001182723.1:p.Asp55Glu
NM_001256819.1:c.165C>G NP_001243748.1:p.Asp55Glu
NM_174878.2:c.165C>G NP_777367.1:p.Asp55Glu
NR_046380.2:n.456C>G
XR_924167.1:n.477C>G
NM_001256819.2:c.165C>G NP_001243748.1:p.Asp55Glu
NM_174878.3:c.165C>G MANE Select NP_777367.1:p.Asp55Glu
NR_046380.3:n.184C>G