Canonical Allele Identifier: CA1410883134
Gene: CLRN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.150927860A= , CM000665.2:g.150927860A= GRCh38
NC_000003.11:g.150645647A= , CM000665.1:g.150645647A= GRCh37
NC_000003.10:g.152128337A= NCBI36
NG_009168.1:g.50140T= , LRG_700:g.50140T=

Transcript Alleles

HGVS Amino-acid change
ENST00000327047.6:c.*76T= MANE Select ENSP00000322280.1:n.*76T=
ENST00000295911.6:c.342+205T= ENSP00000295911.2:n.342+205T=
ENST00000327047.5:c.*76T= ENSP00000322280.1:n.*76T=
ENST00000562308.5:c.104+13722T=
ENST00000565169.1:c.162+13722T=
ENST00000569170.5:c.162+13722T=
NM_001195794.1:c.*76T= , LRG_700t1:c.*76T= NP_001182723.1:n.*76T=
NM_001256819.1:c.*389T= NP_001243748.1:n.*389T=
NM_052995.2:c.342+205T= , LRG_700t2:c.342+205T= NP_443721.1:n.342+205T=
NM_174878.2:c.*76T= NP_777367.1:n.*76T=
NR_046380.2:n.1256T=
XR_924167.1:n.1087T=
NM_001256819.2:c.*389T= NP_001243748.1:n.*389T=
NM_174878.3:c.*76T= MANE Select NP_777367.1:n.*76T=
NR_046380.3:n.984T=