Canonical Allele Identifier: CA355012317

Gene: CLRN1 CLRN1-AS1

Linked Data

• MyVariant Identifiers: chr3:g.150690492G>T (hg19) ; chr3:g.150972705G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.150972705G>T , CM000665.2:g.150972705G>T	GRCh38
NC_000003.11:g.150690492G>T , CM000665.1:g.150690492G>T	GRCh37
NC_000003.10:g.152173182G>T	NCBI36
NG_009168.1:g.5295C>A , LRG_700:g.5295C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327047.6:c.4C>A (CLRN1) MANE Select	ENSP00000322280.1:p.Pro2Thr
ENST00000327047.5:c.4C>A (CLRN1)	ENSP00000322280.1:p.Pro2Thr
ENST00000328863.8:c.4C>A (CLRN1)	ENSP00000329158.4:p.Pro2Thr
ENST00000472224.1:n.10C>A (CLRN1)
NM_001195794.1:c.4C>A , LRG_700t1:c.4C>A (CLRN1)	NP_001182723.1:p.Pro2Thr
NM_001256819.1:c.4C>A (CLRN1)	NP_001243748.1:p.Pro2Thr
NM_174878.2:c.4C>A (CLRN1)	NP_777367.1:p.Pro2Thr
NR_024066.1:n.28G>T (CLRN1-AS1)
NR_046380.2:n.295C>A (CLRN1)
XR_924167.1:n.316C>A (CLRN1)
NR_024066.2:n.28G>T (CLRN1-AS1)
NM_001256819.2:c.4C>A (CLRN1)	NP_001243748.1:p.Pro2Thr
NM_174878.3:c.4C>A (CLRN1) MANE Select	NP_777367.1:p.Pro2Thr
NR_046380.3:n.23C>A (CLRN1)