Canonical Allele Identifier: CA1410910265

Gene: CLRN1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.150972600T= , CM000665.2:g.150972600T=	GRCh38
NC_000003.11:g.150690387T= , CM000665.1:g.150690387T=	GRCh37
NC_000003.10:g.152173077T=	NCBI36
NG_009168.1:g.5400A= , LRG_700:g.5400A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000327047.6:c.109A= MANE Select	ENSP00000322280.1:p.Thr37=
ENST00000468836.2:c.85A=	ENSP00000419892.2:p.Thr29=
ENST00000327047.5:c.109A=	ENSP00000322280.1:p.Thr37=
ENST00000328863.8:c.109A=	ENSP00000329158.4:p.Thr37=
ENST00000468836.1:c.-292A=	ENSP00000419892.1:n.-292A=
ENST00000472224.1:n.115A=
NM_001195794.1:c.109A= , LRG_700t1:c.109A=	NP_001182723.1:p.Thr37=
NM_001256819.1:c.109A=	NP_001243748.1:p.Thr37=
NM_174878.2:c.109A=	NP_777367.1:p.Thr37=
NR_046380.2:n.400A=
XR_924167.1:n.421A=
NM_001256819.2:c.109A=	NP_001243748.1:p.Thr37=
NM_174878.3:c.109A= MANE Select	NP_777367.1:p.Thr37=
NR_046380.3:n.128A=