Canonical Allele Identifier: CA1410910290

Gene: CLRN1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.150972648C= , CM000665.2:g.150972648C=	GRCh38
NC_000003.11:g.150690435C= , CM000665.1:g.150690435C=	GRCh37
NC_000003.10:g.152173125C=	NCBI36
NG_009168.1:g.5352G= , LRG_700:g.5352G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327047.6:c.61G= MANE Select	ENSP00000322280.1:p.Ala21=
ENST00000468836.2:c.37G=	ENSP00000419892.2:p.Ala13=
ENST00000327047.5:c.61G=	ENSP00000322280.1:p.Ala21=
ENST00000328863.8:c.61G=	ENSP00000329158.4:p.Ala21=
ENST00000468836.1:c.-340G=	ENSP00000419892.1:n.-340G=
ENST00000472224.1:n.67G=
NM_001195794.1:c.61G= , LRG_700t1:c.61G=	NP_001182723.1:p.Ala21=
NM_001256819.1:c.61G=	NP_001243748.1:p.Ala21=
NM_174878.2:c.61G=	NP_777367.1:p.Ala21=
NR_046380.2:n.352G=
XR_924167.1:n.373G=
NM_001256819.2:c.61G=	NP_001243748.1:p.Ala21=
NM_174878.3:c.61G= MANE Select	NP_777367.1:p.Ala21=
NR_046380.3:n.80G=