Canonical Allele Identifier: CA1410883257

Gene: CLRN1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.150928149A= , CM000665.2:g.150928149A=	GRCh38
NC_000003.11:g.150645936A= , CM000665.1:g.150645936A=	GRCh37
NC_000003.10:g.152128626A=	NCBI36
NG_009168.1:g.49851T= , LRG_700:g.49851T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327047.6:c.486T= MANE Select	ENSP00000322280.1:p.His162=
ENST00000468836.2:c.634T=	ENSP00000419892.2:n.634T=
ENST00000295911.6:c.258T=	ENSP00000295911.2:p.His86=
ENST00000327047.5:c.486T=	ENSP00000322280.1:p.His162=
ENST00000328863.8:c.525T=	ENSP00000329158.4:p.His175=
ENST00000468836.1:c.258T=	ENSP00000419892.1:p.His86=
ENST00000562308.5:c.104+13433T=
ENST00000565169.1:c.162+13433T=
ENST00000569170.5:c.162+13433T=
NM_001195794.1:c.525T= , LRG_700t1:c.525T=	NP_001182723.1:p.His175=
NM_001256819.1:c.*100T=	NP_001243748.1:n.*100T=
NM_052995.2:c.258T= , LRG_700t2:c.258T=	NP_443721.1:p.His86=
NM_174878.2:c.486T=	NP_777367.1:p.His162=
NR_046380.2:n.967T=
XR_924167.1:n.798T=
NM_001256819.2:c.*100T=	NP_001243748.1:n.*100T=
NM_174878.3:c.486T= MANE Select	NP_777367.1:p.His162=
NR_046380.3:n.695T=