Canonical Allele Identifier: CA1410910201
Gene: CLRN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.150972488C= , CM000665.2:g.150972488C= GRCh38
NC_000003.11:g.150690275C= , CM000665.1:g.150690275C= GRCh37
NC_000003.10:g.152172965C= NCBI36
NG_009168.1:g.5512G= , LRG_700:g.5512G=

Transcript Alleles

HGVS Amino-acid change
ENST00000327047.6:c.221G= MANE Select ENSP00000322280.1:p.Cys74=
ENST00000468836.2:c.197G= ENSP00000419892.2:p.Cys66=
ENST00000644099.1:c.62G= ENSP00000494762.1:p.Cys21=
ENST00000645441.1:c.63G=
ENST00000327047.5:c.221G= ENSP00000322280.1:p.Cys74=
ENST00000328863.8:c.221G= ENSP00000329158.4:p.Cys74=
ENST00000468836.1:c.-180G= ENSP00000419892.1:n.-180G=
ENST00000472224.1:n.227G=
NM_001195794.1:c.221G= , LRG_700t1:c.221G= NP_001182723.1:p.Cys74=
NM_001256819.1:c.221G= NP_001243748.1:p.Cys74=
NM_174878.2:c.221G= NP_777367.1:p.Cys74=
NR_046380.2:n.512G=
XR_924167.1:n.533G=
NM_001256819.2:c.221G= NP_001243748.1:p.Cys74=
NM_174878.3:c.221G= MANE Select NP_777367.1:p.Cys74=
NR_046380.3:n.240G=