Canonical Allele Identifier: CA1410910189

Gene: CLRN1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.150972460G= , CM000665.2:g.150972460G=	GRCh38
NC_000003.11:g.150690247G= , CM000665.1:g.150690247G=	GRCh37
NC_000003.10:g.152172937G=	NCBI36
NG_009168.1:g.5540C= , LRG_700:g.5540C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327047.6:c.249C= MANE Select	ENSP00000322280.1:p.Phe83=
ENST00000468836.2:c.225C=	ENSP00000419892.2:p.Phe75=
ENST00000644099.1:c.90C=	ENSP00000494762.1:p.Phe30=
ENST00000645441.1:c.91C=
ENST00000327047.5:c.249C=	ENSP00000322280.1:p.Phe83=
ENST00000328863.8:c.249C=	ENSP00000329158.4:p.Phe83=
ENST00000468836.1:c.-152C=	ENSP00000419892.1:n.-152C=
ENST00000472224.1:n.255C=
NM_001195794.1:c.249C= , LRG_700t1:c.249C=	NP_001182723.1:p.Phe83=
NM_001256819.1:c.249C=	NP_001243748.1:p.Phe83=
NM_174878.2:c.249C=	NP_777367.1:p.Phe83=
NR_046380.2:n.540C=
XR_924167.1:n.561C=
NM_001256819.2:c.249C=	NP_001243748.1:p.Phe83=
NM_174878.3:c.249C= MANE Select	NP_777367.1:p.Phe83=
NR_046380.3:n.268C=