Canonical Allele Identifier: CA355012211

Gene: CLRN1 CLRN1-AS1

Linked Data

• MyVariant Identifiers: chr3:g.150690467A>T (hg19) ; chr3:g.150972680A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.150972680A>T , CM000665.2:g.150972680A>T	GRCh38
NC_000003.11:g.150690467A>T , CM000665.1:g.150690467A>T	GRCh37
NC_000003.10:g.152173157A>T	NCBI36
NG_009168.1:g.5320T>A , LRG_700:g.5320T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327047.6:c.29T>A (CLRN1) MANE Select	ENSP00000322280.1:p.Phe10Tyr
ENST00000468836.2:c.5T>A (CLRN1)	ENSP00000419892.2:p.Phe2Tyr
ENST00000327047.5:c.29T>A (CLRN1)	ENSP00000322280.1:p.Phe10Tyr
ENST00000328863.8:c.29T>A (CLRN1)	ENSP00000329158.4:p.Phe10Tyr
ENST00000468836.1:c.-372T>A (CLRN1)	ENSP00000419892.1:n.-372T>A
ENST00000472224.1:n.35T>A (CLRN1)
NM_001195794.1:c.29T>A , LRG_700t1:c.29T>A (CLRN1)	NP_001182723.1:p.Phe10Tyr
NM_001256819.1:c.29T>A (CLRN1)	NP_001243748.1:p.Phe10Tyr
NM_174878.2:c.29T>A (CLRN1)	NP_777367.1:p.Phe10Tyr
NR_024066.1:n.3A>T (CLRN1-AS1)
NR_046380.2:n.320T>A (CLRN1)
XR_924167.1:n.341T>A (CLRN1)
NR_024066.2:n.3A>T (CLRN1-AS1)
NM_001256819.2:c.29T>A (CLRN1)	NP_001243748.1:p.Phe10Tyr
NM_174878.3:c.29T>A (CLRN1) MANE Select	NP_777367.1:p.Phe10Tyr
NR_046380.3:n.48T>A (CLRN1)