Canonical Allele Identifier: CA85947810

Gene: CLRN1

Linked Data

• ClinVar Variation Id: 2171637
• ClinVar RCV Id: RCV003087019
• dbSNP Id: rs1013290166
• gnomAD v2: 3-150690252-G-C
• gnomAD v3: 3-150972465-G-C
• gnomAD v4: 3-150972465-G-C
• MyVariant Identifiers: chr3:g.150690252G>C (hg19) ; chr3:g.150972465G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.150972465G>C , CM000665.2:g.150972465G>C	GRCh38
NC_000003.11:g.150690252G>C , CM000665.1:g.150690252G>C	GRCh37
NC_000003.10:g.152172942G>C	NCBI36
NG_009168.1:g.5535C>G , LRG_700:g.5535C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327047.6:c.244C>G MANE Select	ENSP00000322280.1:p.Arg82Gly
ENST00000468836.2:c.220C>G	ENSP00000419892.2:p.Arg74Gly
ENST00000644099.1:c.85C>G	ENSP00000494762.1:p.Arg29Gly
ENST00000645441.1:c.86C>G
ENST00000327047.5:c.244C>G	ENSP00000322280.1:p.Arg82Gly
ENST00000328863.8:c.244C>G	ENSP00000329158.4:p.Arg82Gly
ENST00000468836.1:c.-157C>G	ENSP00000419892.1:n.-157C>G
ENST00000472224.1:n.250C>G
NM_001195794.1:c.244C>G , LRG_700t1:c.244C>G	NP_001182723.1:p.Arg82Gly
NM_001256819.1:c.244C>G	NP_001243748.1:p.Arg82Gly
NM_174878.2:c.244C>G	NP_777367.1:p.Arg82Gly
NR_046380.2:n.535C>G
XR_924167.1:n.556C>G
NM_001256819.2:c.244C>G	NP_001243748.1:p.Arg82Gly
NM_174878.3:c.244C>G MANE Select	NP_777367.1:p.Arg82Gly
NR_046380.3:n.263C>G