Canonical Allele Identifier: CA1410888478

Gene: CLRN1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.150941609C= , CM000665.2:g.150941609C=	GRCh38
NC_000003.11:g.150659396C= , CM000665.1:g.150659396C=	GRCh37
NC_000003.10:g.152142086C=	NCBI36
NG_009168.1:g.36391G= , LRG_700:g.36391G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327047.6:c.406G= MANE Select	ENSP00000322280.1:p.Gly136=
ENST00000468836.2:c.554G=	ENSP00000419892.2:n.554G=
ENST00000644099.1:c.398G=	ENSP00000494762.1:n.398G=
ENST00000295911.6:c.178G=	ENSP00000295911.2:p.Gly60=
ENST00000327047.5:c.406G=	ENSP00000322280.1:p.Gly136=
ENST00000328863.8:c.406G=	ENSP00000329158.4:p.Gly136=
ENST00000468836.1:c.178G=	ENSP00000419892.1:p.Gly60=
ENST00000472224.1:n.412G=
ENST00000485607.1:c.70G=	ENSP00000419244.1:p.Gly24=
ENST00000562308.5:c.77G=
ENST00000565169.1:c.135G=
ENST00000569170.5:c.135G=
NM_001195794.1:c.406G= , LRG_700t1:c.406G=	NP_001182723.1:p.Gly136=
NM_001256819.1:c.*20G=	NP_001243748.1:n.*20G=
NM_052995.2:c.178G= , LRG_700t2:c.178G=	NP_443721.1:p.Gly60=
NM_174878.2:c.406G=	NP_777367.1:p.Gly136=
NR_046380.2:n.848G=
XR_924167.1:n.718G=
NM_001256819.2:c.*20G=	NP_001243748.1:n.*20G=
NM_174878.3:c.406G= MANE Select	NP_777367.1:p.Gly136=
NR_046380.3:n.576G=