Canonical Allele Identifier: CA1410883132
Gene: CLRN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.150927858G= , CM000665.2:g.150927858G= GRCh38
NC_000003.11:g.150645645G= , CM000665.1:g.150645645G= GRCh37
NC_000003.10:g.152128335G= NCBI36
NG_009168.1:g.50142C= , LRG_700:g.50142C=

Transcript Alleles

HGVS Amino-acid change
ENST00000327047.6:c.*78C= MANE Select ENSP00000322280.1:n.*78C=
ENST00000295911.6:c.342+207C= ENSP00000295911.2:n.342+207C=
ENST00000327047.5:c.*78C= ENSP00000322280.1:n.*78C=
ENST00000562308.5:c.104+13724C=
ENST00000565169.1:c.162+13724C=
ENST00000569170.5:c.162+13724C=
NM_001195794.1:c.*78C= , LRG_700t1:c.*78C= NP_001182723.1:n.*78C=
NM_001256819.1:c.*391C= NP_001243748.1:n.*391C=
NM_052995.2:c.342+207C= , LRG_700t2:c.342+207C= NP_443721.1:n.342+207C=
NM_174878.2:c.*78C= NP_777367.1:n.*78C=
NR_046380.2:n.1258C=
XR_924167.1:n.1089C=
NM_001256819.2:c.*391C= NP_001243748.1:n.*391C=
NM_174878.3:c.*78C= MANE Select NP_777367.1:n.*78C=
NR_046380.3:n.986C=