Canonical Allele Identifier: CA1410910200

Gene: CLRN1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.150972487A= , CM000665.2:g.150972487A=	GRCh38
NC_000003.11:g.150690274A= , CM000665.1:g.150690274A=	GRCh37
NC_000003.10:g.152172964A=	NCBI36
NG_009168.1:g.5513T= , LRG_700:g.5513T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327047.6:c.222T= MANE Select	ENSP00000322280.1:p.Cys74=
ENST00000468836.2:c.198T=	ENSP00000419892.2:p.Cys66=
ENST00000644099.1:c.63T=	ENSP00000494762.1:p.Cys21=
ENST00000645441.1:c.64T=
ENST00000327047.5:c.222T=	ENSP00000322280.1:p.Cys74=
ENST00000328863.8:c.222T=	ENSP00000329158.4:p.Cys74=
ENST00000468836.1:c.-179T=	ENSP00000419892.1:n.-179T=
ENST00000472224.1:n.228T=
NM_001195794.1:c.222T= , LRG_700t1:c.222T=	NP_001182723.1:p.Cys74=
NM_001256819.1:c.222T=	NP_001243748.1:p.Cys74=
NM_174878.2:c.222T=	NP_777367.1:p.Cys74=
NR_046380.2:n.513T=
XR_924167.1:n.534T=
NM_001256819.2:c.222T=	NP_001243748.1:p.Cys74=
NM_174878.3:c.222T= MANE Select	NP_777367.1:p.Cys74=
NR_046380.3:n.241T=