Canonical Allele Identifier: CA1410910314
Community Standard Title: NM_174878.3(CLRN1):c.13C= (p.Gln5=)
Gene: CLRN1 HGNC NCBI
CLRN1-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.150972696G= , CM000665.2:g.150972696G= GRCh38
NC_000003.11:g.150690483G= , CM000665.1:g.150690483G= GRCh37
NC_000003.10:g.152173173G= NCBI36
NG_009168.1:g.5304C= , LRG_700:g.5304C=

Transcript Alleles

HGVS Amino-acid Change
NM_174878.3:c.13C= (CLRN1) MANE Select NP_777367.1:p.Gln5=
ENST00000327047.6:c.13C= (CLRN1) MANE Select ENSP00000322280.1:p.Gln5=
NM_001195794.1:c.13C= , LRG_700t1:c.13C= (CLRN1) NP_001182723.1:p.Gln5=
NM_001256819.1:c.13C= (CLRN1) NP_001243748.1:p.Gln5=
NM_001256819.2:c.13C= (CLRN1) NP_001243748.1:p.Gln5=
NM_174878.2:c.13C= (CLRN1) NP_777367.1:p.Gln5=
NR_024066.1:n.19G= (CLRN1-AS1)
NR_024066.2:n.19G= (CLRN1-AS1)
NR_046380.2:n.304C= (CLRN1)
NR_046380.3:n.32C= (CLRN1)
ENST00000327047.5:c.13C= (CLRN1) ENSP00000322280.1:p.Gln5=
ENST00000328863.8:c.13C= (CLRN1) ENSP00000329158.4:p.Gln5=
ENST00000472224.1:n.19C= (CLRN1)
XR_924167.1:n.325C= (CLRN1)