Canonical Allele Identifier: CA1410910193

Gene: CLRN1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.150972466A= , CM000665.2:g.150972466A=	GRCh38
NC_000003.11:g.150690253A= , CM000665.1:g.150690253A=	GRCh37
NC_000003.10:g.152172943A=	NCBI36
NG_009168.1:g.5534T= , LRG_700:g.5534T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327047.6:c.243T= MANE Select	ENSP00000322280.1:p.Phe81=
ENST00000468836.2:c.219T=	ENSP00000419892.2:p.Phe73=
ENST00000644099.1:c.84T=	ENSP00000494762.1:p.Phe28=
ENST00000645441.1:c.85T=
ENST00000327047.5:c.243T=	ENSP00000322280.1:p.Phe81=
ENST00000328863.8:c.243T=	ENSP00000329158.4:p.Phe81=
ENST00000468836.1:c.-158T=	ENSP00000419892.1:n.-158T=
ENST00000472224.1:n.249T=
NM_001195794.1:c.243T= , LRG_700t1:c.243T=	NP_001182723.1:p.Phe81=
NM_001256819.1:c.243T=	NP_001243748.1:p.Phe81=
NM_174878.2:c.243T=	NP_777367.1:p.Phe81=
NR_046380.2:n.534T=
XR_924167.1:n.555T=
NM_001256819.2:c.243T=	NP_001243748.1:p.Phe81=
NM_174878.3:c.243T= MANE Select	NP_777367.1:p.Phe81=
NR_046380.3:n.262T=