Canonical Allele Identifier: CA1410883229

Gene: CLRN1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.150928079T= , CM000665.2:g.150928079T=	GRCh38
NC_000003.11:g.150645866T= , CM000665.1:g.150645866T=	GRCh37
NC_000003.10:g.152128556T=	NCBI36
NG_009168.1:g.49921A= , LRG_700:g.49921A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000327047.6:c.556A= MANE Select	ENSP00000322280.1:p.Thr186=
ENST00000468836.2:c.704A=	ENSP00000419892.2:n.704A=
ENST00000295911.6:c.328A=	ENSP00000295911.2:p.Thr110=
ENST00000327047.5:c.556A=	ENSP00000322280.1:p.Thr186=
ENST00000328863.8:c.595A=	ENSP00000329158.4:p.Thr199=
ENST00000468836.1:c.328A=	ENSP00000419892.1:p.Thr110=
ENST00000562308.5:c.104+13503A=
ENST00000565169.1:c.162+13503A=
ENST00000569170.5:c.162+13503A=
NM_001195794.1:c.595A= , LRG_700t1:c.595A=	NP_001182723.1:p.Thr199=
NM_001256819.1:c.*170A=	NP_001243748.1:n.*170A=
NM_052995.2:c.328A= , LRG_700t2:c.328A=	NP_443721.1:p.Thr110=
NM_174878.2:c.556A=	NP_777367.1:p.Thr186=
NR_046380.2:n.1037A=
XR_924167.1:n.868A=
NM_001256819.2:c.*170A=	NP_001243748.1:n.*170A=
NM_174878.3:c.556A= MANE Select	NP_777367.1:p.Thr186=
NR_046380.3:n.765A=