Canonical Allele Identifier: CA355012200
Gene: CLRN1 HGNC NCBI
CLRN1-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.150972678A>T , CM000665.2:g.150972678A>T GRCh38
NC_000003.11:g.150690465A>T , CM000665.1:g.150690465A>T GRCh37
NC_000003.10:g.152173155A>T NCBI36
NG_009168.1:g.5322T>A , LRG_700:g.5322T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000327047.6:c.31T>A (CLRN1) MANE Select ENSP00000322280.1:p.Cys11Ser
ENST00000468836.2:c.7T>A (CLRN1) ENSP00000419892.2:p.Cys3Ser
ENST00000327047.5:c.31T>A (CLRN1) ENSP00000322280.1:p.Cys11Ser
ENST00000328863.8:c.31T>A (CLRN1) ENSP00000329158.4:p.Cys11Ser
ENST00000468836.1:c.-370T>A (CLRN1) ENSP00000419892.1:n.-370T>A
ENST00000472224.1:n.37T>A (CLRN1)
NM_001195794.1:c.31T>A , LRG_700t1:c.31T>A (CLRN1) NP_001182723.1:p.Cys11Ser
NM_001256819.1:c.31T>A (CLRN1) NP_001243748.1:p.Cys11Ser
NM_174878.2:c.31T>A (CLRN1) NP_777367.1:p.Cys11Ser
NR_024066.1:n.1A>T (CLRN1-AS1)
NR_046380.2:n.322T>A (CLRN1)
XR_924167.1:n.343T>A (CLRN1)
NR_024066.2:n.1A>T (CLRN1-AS1)
NM_001256819.2:c.31T>A (CLRN1) NP_001243748.1:p.Cys11Ser
NM_174878.3:c.31T>A (CLRN1) MANE Select NP_777367.1:p.Cys11Ser
NR_046380.3:n.50T>A (CLRN1)