Canonical Allele Identifier: CA1410888481

Gene: CLRN1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.150941616A= , CM000665.2:g.150941616A=	GRCh38
NC_000003.11:g.150659403A= , CM000665.1:g.150659403A=	GRCh37
NC_000003.10:g.152142093A=	NCBI36
NG_009168.1:g.36384T= , LRG_700:g.36384T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327047.6:c.399T= MANE Select	ENSP00000322280.1:p.Gly133=
ENST00000468836.2:c.547T=	ENSP00000419892.2:n.547T=
ENST00000644099.1:c.391T=	ENSP00000494762.1:n.391T=
ENST00000295911.6:c.171T=	ENSP00000295911.2:p.Gly57=
ENST00000327047.5:c.399T=	ENSP00000322280.1:p.Gly133=
ENST00000328863.8:c.399T=	ENSP00000329158.4:p.Gly133=
ENST00000468836.1:c.171T=	ENSP00000419892.1:p.Gly57=
ENST00000472224.1:n.405T=
ENST00000485607.1:c.63T=	ENSP00000419244.1:p.Gly21=
ENST00000562308.5:c.70T=
ENST00000565169.1:c.128T=
ENST00000569170.5:c.128T=
NM_001195794.1:c.399T= , LRG_700t1:c.399T=	NP_001182723.1:p.Gly133=
NM_001256819.1:c.*13T=	NP_001243748.1:n.*13T=
NM_052995.2:c.171T= , LRG_700t2:c.171T=	NP_443721.1:p.Gly57=
NM_174878.2:c.399T=	NP_777367.1:p.Gly133=
NR_046380.2:n.841T=
XR_924167.1:n.711T=
NM_001256819.2:c.*13T=	NP_001243748.1:n.*13T=
NM_174878.3:c.399T= MANE Select	NP_777367.1:p.Gly133=
NR_046380.3:n.569T=