Canonical Allele Identifier: CA436403264

Gene: CLRN1 CLRN1-AS1

Linked Data

• MyVariant Identifiers: chr3:g.150690490T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.150972703T>A , CM000665.2:g.150972703T>A	GRCh38
NC_000003.11:g.150690490T>A , CM000665.1:g.150690490T>A	GRCh37
NC_000003.10:g.152173180T>A	NCBI36
NG_009168.1:g.5297A>T , LRG_700:g.5297A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327047.6:c.6A>T (CLRN1) MANE Select	ENSP00000322280.1:p.Pro2=
ENST00000327047.5:c.6A>T (CLRN1)	ENSP00000322280.1:p.Pro2=
ENST00000328863.8:c.6A>T (CLRN1)	ENSP00000329158.4:p.Pro2=
ENST00000472224.1:n.12A>T (CLRN1)
NM_001195794.1:c.6A>T , LRG_700t1:c.6A>T (CLRN1)	NP_001182723.1:p.Pro2=
NM_001256819.1:c.6A>T (CLRN1)	NP_001243748.1:p.Pro2=
NM_174878.2:c.6A>T (CLRN1)	NP_777367.1:p.Pro2=
NR_024066.1:n.26T>A (CLRN1-AS1)
NR_046380.2:n.297A>T (CLRN1)
XR_924167.1:n.318A>T (CLRN1)
NR_024066.2:n.26T>A (CLRN1-AS1)
NM_001256819.2:c.6A>T (CLRN1)	NP_001243748.1:p.Pro2=
NM_174878.3:c.6A>T (CLRN1) MANE Select	NP_777367.1:p.Pro2=
NR_046380.3:n.25A>T (CLRN1)