Canonical Allele Identifier: CA1410910223
Gene: CLRN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.150972531C= , CM000665.2:g.150972531C= GRCh38
NC_000003.11:g.150690318C= , CM000665.1:g.150690318C= GRCh37
NC_000003.10:g.152173008C= NCBI36
NG_009168.1:g.5469G= , LRG_700:g.5469G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000327047.6:c.178G= MANE Select ENSP00000322280.1:p.Glu60=
ENST00000468836.2:c.154G= ENSP00000419892.2:p.Glu52=
ENST00000644099.1:c.19G= ENSP00000494762.1:p.Glu7=
ENST00000645441.1:c.20G=
ENST00000327047.5:c.178G= ENSP00000322280.1:p.Glu60=
ENST00000328863.8:c.178G= ENSP00000329158.4:p.Glu60=
ENST00000468836.1:c.-223G= ENSP00000419892.1:n.-223G=
ENST00000472224.1:n.184G=
NM_001195794.1:c.178G= , LRG_700t1:c.178G= NP_001182723.1:p.Glu60=
NM_001256819.1:c.178G= NP_001243748.1:p.Glu60=
NM_174878.2:c.178G= NP_777367.1:p.Glu60=
NR_046380.2:n.469G=
XR_924167.1:n.490G=
NM_001256819.2:c.178G= NP_001243748.1:p.Glu60=
NM_174878.3:c.178G= MANE Select NP_777367.1:p.Glu60=
NR_046380.3:n.197G=