Canonical Allele Identifier: CA1410888477

Gene: CLRN1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.150941608C= , CM000665.2:g.150941608C=	GRCh38
NC_000003.11:g.150659395C= , CM000665.1:g.150659395C=	GRCh37
NC_000003.10:g.152142085C=	NCBI36
NG_009168.1:g.36392G= , LRG_700:g.36392G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327047.6:c.407G= MANE Select	ENSP00000322280.1:p.Gly136=
ENST00000468836.2:c.555G=	ENSP00000419892.2:n.555G=
ENST00000644099.1:c.399G=	ENSP00000494762.1:n.399G=
ENST00000295911.6:c.179G=	ENSP00000295911.2:p.Gly60=
ENST00000327047.5:c.407G=	ENSP00000322280.1:p.Gly136=
ENST00000328863.8:c.407G=	ENSP00000329158.4:p.Gly136=
ENST00000468836.1:c.179G=	ENSP00000419892.1:p.Gly60=
ENST00000472224.1:n.413G=
ENST00000485607.1:c.71G=	ENSP00000419244.1:p.Gly24=
ENST00000562308.5:c.78G=
ENST00000565169.1:c.136G=
ENST00000569170.5:c.136G=
NM_001195794.1:c.407G= , LRG_700t1:c.407G=	NP_001182723.1:p.Gly136=
NM_001256819.1:c.*21G=	NP_001243748.1:n.*21G=
NM_052995.2:c.179G= , LRG_700t2:c.179G=	NP_443721.1:p.Gly60=
NM_174878.2:c.407G=	NP_777367.1:p.Gly136=
NR_046380.2:n.849G=
XR_924167.1:n.719G=
NM_001256819.2:c.*21G=	NP_001243748.1:n.*21G=
NM_174878.3:c.407G= MANE Select	NP_777367.1:p.Gly136=
NR_046380.3:n.577G=