Canonical Allele Identifier: CA1410910232

Gene: CLRN1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.150972548A= , CM000665.2:g.150972548A=	GRCh38
NC_000003.11:g.150690335A= , CM000665.1:g.150690335A=	GRCh37
NC_000003.10:g.152173025A=	NCBI36
NG_009168.1:g.5452T= , LRG_700:g.5452T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327047.6:c.161T= MANE Select	ENSP00000322280.1:p.Leu54=
ENST00000468836.2:c.137T=	ENSP00000419892.2:p.Leu46=
ENST00000644099.1:c.2T=	ENSP00000494762.1:p.Leu1=
ENST00000645441.1:c.3T=
ENST00000327047.5:c.161T=	ENSP00000322280.1:p.Leu54=
ENST00000328863.8:c.161T=	ENSP00000329158.4:p.Leu54=
ENST00000468836.1:c.-240T=	ENSP00000419892.1:n.-240T=
ENST00000472224.1:n.167T=
NM_001195794.1:c.161T= , LRG_700t1:c.161T=	NP_001182723.1:p.Leu54=
NM_001256819.1:c.161T=	NP_001243748.1:p.Leu54=
NM_174878.2:c.161T=	NP_777367.1:p.Leu54=
NR_046380.2:n.452T=
XR_924167.1:n.473T=
NM_001256819.2:c.161T=	NP_001243748.1:p.Leu54=
NM_174878.3:c.161T= MANE Select	NP_777367.1:p.Leu54=
NR_046380.3:n.180T=