Canonical Allele Identifier: CA1410910211

Gene: CLRN1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.150972513A= , CM000665.2:g.150972513A=	GRCh38
NC_000003.11:g.150690300A= , CM000665.1:g.150690300A=	GRCh37
NC_000003.10:g.152172990A=	NCBI36
NG_009168.1:g.5487T= , LRG_700:g.5487T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327047.6:c.196T= MANE Select	ENSP00000322280.1:p.Phe66=
ENST00000468836.2:c.172T=	ENSP00000419892.2:p.Phe58=
ENST00000644099.1:c.37T=	ENSP00000494762.1:p.Phe13=
ENST00000645441.1:c.38T=
ENST00000327047.5:c.196T=	ENSP00000322280.1:p.Phe66=
ENST00000328863.8:c.196T=	ENSP00000329158.4:p.Phe66=
ENST00000468836.1:c.-205T=	ENSP00000419892.1:n.-205T=
ENST00000472224.1:n.202T=
NM_001195794.1:c.196T= , LRG_700t1:c.196T=	NP_001182723.1:p.Phe66=
NM_001256819.1:c.196T=	NP_001243748.1:p.Phe66=
NM_174878.2:c.196T=	NP_777367.1:p.Phe66=
NR_046380.2:n.487T=
XR_924167.1:n.508T=
NM_001256819.2:c.196T=	NP_001243748.1:p.Phe66=
NM_174878.3:c.196T= MANE Select	NP_777367.1:p.Phe66=
NR_046380.3:n.215T=