Canonical Allele Identifier: CA354953083

Gene: CLRN1

Linked Data

• MyVariant Identifiers: chr3:g.150645875C>A (hg19) ; chr3:g.150928088C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.150928088C>A , CM000665.2:g.150928088C>A	GRCh38
NC_000003.11:g.150645875C>A , CM000665.1:g.150645875C>A	GRCh37
NC_000003.10:g.152128565C>A	NCBI36
NG_009168.1:g.49912G>T , LRG_700:g.49912G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000327047.6:c.547G>T MANE Select	ENSP00000322280.1:p.Glu183Ter
ENST00000468836.2:c.695G>T	ENSP00000419892.2:n.695G>T
ENST00000295911.6:c.319G>T	ENSP00000295911.2:p.Glu107Ter
ENST00000327047.5:c.547G>T	ENSP00000322280.1:p.Glu183Ter
ENST00000328863.8:c.586G>T	ENSP00000329158.4:p.Glu196Ter
ENST00000468836.1:c.319G>T	ENSP00000419892.1:p.Glu107Ter
ENST00000562308.5:c.104+13494G>T
ENST00000565169.1:c.162+13494G>T
ENST00000569170.5:c.162+13494G>T
NM_001195794.1:c.586G>T , LRG_700t1:c.586G>T	NP_001182723.1:p.Glu196Ter
NM_001256819.1:c.*161G>T	NP_001243748.1:n.*161G>T
NM_052995.2:c.319G>T , LRG_700t2:c.319G>T	NP_443721.1:p.Glu107Ter
NM_174878.2:c.547G>T	NP_777367.1:p.Glu183Ter
NR_046380.2:n.1028G>T
XR_924167.1:n.859G>T
NM_001256819.2:c.*161G>T	NP_001243748.1:n.*161G>T
NM_174878.3:c.547G>T MANE Select	NP_777367.1:p.Glu183Ter
NR_046380.3:n.756G>T