Canonical Allele Identifier: CA354953059

Gene: CLRN1

Linked Data

• ClinVar Variation Id: 1349938
• ClinVar RCV Id: RCV002039377
• dbSNP Id: rs2107927838
• MyVariant Identifiers: chr3:g.150645865G>T (hg19) ; chr3:g.150928078G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.150928078G>T , CM000665.2:g.150928078G>T	GRCh38
NC_000003.11:g.150645865G>T , CM000665.1:g.150645865G>T	GRCh37
NC_000003.10:g.152128555G>T	NCBI36
NG_009168.1:g.49922C>A , LRG_700:g.49922C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000327047.6:c.557C>A MANE Select	ENSP00000322280.1:p.Thr186Asn
ENST00000468836.2:c.705C>A	ENSP00000419892.2:n.705C>A
ENST00000295911.6:c.329C>A	ENSP00000295911.2:p.Thr110Asn
ENST00000327047.5:c.557C>A	ENSP00000322280.1:p.Thr186Asn
ENST00000328863.8:c.596C>A	ENSP00000329158.4:p.Thr199Asn
ENST00000468836.1:c.329C>A	ENSP00000419892.1:p.Thr110Asn
ENST00000562308.5:c.104+13504C>A
ENST00000565169.1:c.162+13504C>A
ENST00000569170.5:c.162+13504C>A
NM_001195794.1:c.596C>A , LRG_700t1:c.596C>A	NP_001182723.1:p.Thr199Asn
NM_001256819.1:c.*171C>A	NP_001243748.1:n.*171C>A
NM_052995.2:c.329C>A , LRG_700t2:c.329C>A	NP_443721.1:p.Thr110Asn
NM_174878.2:c.557C>A	NP_777367.1:p.Thr186Asn
NR_046380.2:n.1038C>A
XR_924167.1:n.869C>A
NM_001256819.2:c.*171C>A	NP_001243748.1:n.*171C>A
NM_174878.3:c.557C>A MANE Select	NP_777367.1:p.Thr186Asn
NR_046380.3:n.766C>A