Canonical Allele Identifier: CA547369140

Gene: CLRN1

Linked Data

• dbSNP Id: rs1397302437
• gnomAD v2: 3-150690205-C-G
• gnomAD v3: 3-150972418-C-G
• gnomAD v4: 3-150972418-C-G
• MyVariant Identifiers: chr3:g.150690205C>G (hg19) ; chr3:g.150690205_150690206delinsGT (hg19) ; chr3:g.150972418C>G (hg38) ; chr3:g.150972418_150972419delinsGT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.150972418C>G , CM000665.2:g.150972418C>G	GRCh38
NC_000003.11:g.150690205C>G , CM000665.1:g.150690205C>G	GRCh37
NC_000003.10:g.152172895C>G	NCBI36
NG_009168.1:g.5582G>C , LRG_700:g.5582G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327047.6:c.253+38G>C MANE Select	ENSP00000322280.1:n.253+38G>C
ENST00000468836.2:c.229+38G>C	ENSP00000419892.2:n.229+38G>C
ENST00000644099.1:c.94+38G>C	ENSP00000494762.1:n.94+38G>C
ENST00000645441.1:c.95+38G>C
ENST00000327047.5:c.253+38G>C	ENSP00000322280.1:n.253+38G>C
ENST00000328863.8:c.253+38G>C	ENSP00000329158.4:n.253+38G>C
ENST00000468836.1:c.-148+38G>C	ENSP00000419892.1:n.-148+38G>C
ENST00000472224.1:n.259+38G>C
NM_001195794.1:c.253+38G>C , LRG_700t1:c.253+38G>C	NP_001182723.1:n.253+38G>C
NM_001256819.1:c.253+38G>C	NP_001243748.1:n.253+38G>C
NM_174878.2:c.253+38G>C	NP_777367.1:n.253+38G>C
NR_046380.2:n.544+38G>C
XR_924167.1:n.565+38G>C
NM_001256819.2:c.253+38G>C	NP_001243748.1:n.253+38G>C
NM_174878.3:c.253+38G>C MANE Select	NP_777367.1:n.253+38G>C
NR_046380.3:n.272+38G>C