Canonical Allele Identifier: CA355012305
Gene: CLRN1 HGNC NCBI
CLRN1-AS1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.150690489T>G (hg19) chr3:g.150972702T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.150972702T>G , CM000665.2:g.150972702T>G GRCh38
NC_000003.11:g.150690489T>G , CM000665.1:g.150690489T>G GRCh37
NC_000003.10:g.152173179T>G NCBI36
NG_009168.1:g.5298A>C , LRG_700:g.5298A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000327047.6:c.7A>C (CLRN1) MANE Select ENSP00000322280.1:p.Ser3Arg
ENST00000327047.5:c.7A>C (CLRN1) ENSP00000322280.1:p.Ser3Arg
ENST00000328863.8:c.7A>C (CLRN1) ENSP00000329158.4:p.Ser3Arg
ENST00000472224.1:n.13A>C (CLRN1)
NM_001195794.1:c.7A>C , LRG_700t1:c.7A>C (CLRN1) NP_001182723.1:p.Ser3Arg
NM_001256819.1:c.7A>C (CLRN1) NP_001243748.1:p.Ser3Arg
NM_174878.2:c.7A>C (CLRN1) NP_777367.1:p.Ser3Arg
NR_024066.1:n.25T>G (CLRN1-AS1)
NR_046380.2:n.298A>C (CLRN1)
XR_924167.1:n.319A>C (CLRN1)
NR_024066.2:n.25T>G (CLRN1-AS1)
NM_001256819.2:c.7A>C (CLRN1) NP_001243748.1:p.Ser3Arg
NM_174878.3:c.7A>C (CLRN1) MANE Select NP_777367.1:p.Ser3Arg
NR_046380.3:n.26A>C (CLRN1)
Search 100 bp 5'
Search 100 bp 3'