Canonical Allele Identifier: CA2668198821
Gene: CLRN1 HGNC NCBI
CLRN1-AS1 HGNC NCBI

Linked Data

gnomAD v4: 3-150972696-GTTGGC-G
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.150972702_150972706del , CM000665.2:g.150972702_150972706del GRCh38
NC_000003.11:g.150690489_150690493del , CM000665.1:g.150690489_150690493del GRCh37
NC_000003.10:g.152173179_152173183del NCBI36
NG_009168.1:g.5299_5303del , LRG_700:g.5299_5303del

Transcript Alleles

HGVS Amino-acid Change
ENST00000327047.6:c.8_12del (CLRN1) MANE Select ENSP00000322280.1:p.Ser3ThrfsTer?
ENST00000327047.5:c.8_12del (CLRN1) ENSP00000322280.1:p.Ser3ThrfsTer?
ENST00000328863.8:c.8_12del (CLRN1) ENSP00000329158.4:p.Ser3ThrfsTer?
ENST00000472224.1:n.14_18del (CLRN1)
NM_001195794.1:c.8_12del , LRG_700t1:c.8_12del (CLRN1) NP_001182723.1:p.Ser3ThrfsTer?
NM_001256819.1:c.8_12del (CLRN1) NP_001243748.1:p.Ser3ThrfsTer?
NM_174878.2:c.8_12del (CLRN1) NP_777367.1:p.Ser3ThrfsTer?
NR_024066.1:n.25_29del (CLRN1-AS1)
NR_046380.2:n.299_303del (CLRN1)
XR_924167.1:n.320_324del (CLRN1)
NR_024066.2:n.25_29del (CLRN1-AS1)
NM_001256819.2:c.8_12del (CLRN1) NP_001243748.1:p.Ser3ThrfsTer?
NM_174878.3:c.8_12del (CLRN1) MANE Select NP_777367.1:p.Ser3ThrfsTer?
NR_046380.3:n.27_31del (CLRN1)
Search 100 bp 5'
Search 100 bp 3'