Canonical Allele Identifier: CA1410883259

Gene: CLRN1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.150928155T= , CM000665.2:g.150928155T=	GRCh38
NC_000003.11:g.150645942T= , CM000665.1:g.150645942T=	GRCh37
NC_000003.10:g.152128632T=	NCBI36
NG_009168.1:g.49845A= , LRG_700:g.49845A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327047.6:c.480A= MANE Select	ENSP00000322280.1:p.Lys160=
ENST00000468836.2:c.628A=	ENSP00000419892.2:n.628A=
ENST00000295911.6:c.252A=	ENSP00000295911.2:p.Lys84=
ENST00000327047.5:c.480A=	ENSP00000322280.1:p.Lys160=
ENST00000328863.8:c.519A=	ENSP00000329158.4:p.Lys173=
ENST00000468836.1:c.252A=	ENSP00000419892.1:p.Lys84=
ENST00000562308.5:c.104+13427A=
ENST00000565169.1:c.162+13427A=
ENST00000569170.5:c.162+13427A=
NM_001195794.1:c.519A= , LRG_700t1:c.519A=	NP_001182723.1:p.Lys173=
NM_001256819.1:c.*94A=	NP_001243748.1:n.*94A=
NM_052995.2:c.252A= , LRG_700t2:c.252A=	NP_443721.1:p.Lys84=
NM_174878.2:c.480A=	NP_777367.1:p.Lys160=
NR_046380.2:n.961A=
XR_924167.1:n.792A=
NM_001256819.2:c.*94A=	NP_001243748.1:n.*94A=
NM_174878.3:c.480A= MANE Select	NP_777367.1:p.Lys160=
NR_046380.3:n.689A=