Canonical Allele Identifier: CA1410910228

Gene: CLRN1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.150972543T= , CM000665.2:g.150972543T=	GRCh38
NC_000003.11:g.150690330T= , CM000665.1:g.150690330T=	GRCh37
NC_000003.10:g.152173020T=	NCBI36
NG_009168.1:g.5457A= , LRG_700:g.5457A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327047.6:c.166A= MANE Select	ENSP00000322280.1:p.Lys56=
ENST00000468836.2:c.142A=	ENSP00000419892.2:p.Lys48=
ENST00000644099.1:c.7A=	ENSP00000494762.1:p.Lys3=
ENST00000645441.1:c.8A=
ENST00000327047.5:c.166A=	ENSP00000322280.1:p.Lys56=
ENST00000328863.8:c.166A=	ENSP00000329158.4:p.Lys56=
ENST00000468836.1:c.-235A=	ENSP00000419892.1:n.-235A=
ENST00000472224.1:n.172A=
NM_001195794.1:c.166A= , LRG_700t1:c.166A=	NP_001182723.1:p.Lys56=
NM_001256819.1:c.166A=	NP_001243748.1:p.Lys56=
NM_174878.2:c.166A=	NP_777367.1:p.Lys56=
NR_046380.2:n.457A=
XR_924167.1:n.478A=
NM_001256819.2:c.166A=	NP_001243748.1:p.Lys56=
NM_174878.3:c.166A= MANE Select	NP_777367.1:p.Lys56=
NR_046380.3:n.185A=