Canonical Allele Identifier: CA1410888500

Gene: CLRN1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.150941659A= , CM000665.2:g.150941659A=	GRCh38
NC_000003.11:g.150659446A= , CM000665.1:g.150659446A=	GRCh37
NC_000003.10:g.152142136A=	NCBI36
NG_009168.1:g.36341T= , LRG_700:g.36341T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000327047.6:c.356T= MANE Select	ENSP00000322280.1:p.Phe119=
ENST00000468836.2:c.504T=	ENSP00000419892.2:p.Leu168=
ENST00000644099.1:c.348T=	ENSP00000494762.1:n.348T=
ENST00000295911.6:c.128T=	ENSP00000295911.2:p.Phe43=
ENST00000327047.5:c.356T=	ENSP00000322280.1:p.Phe119=
ENST00000328863.8:c.356T=	ENSP00000329158.4:p.Phe119=
ENST00000468836.1:c.128T=	ENSP00000419892.1:p.Phe43=
ENST00000472224.1:n.362T=
ENST00000485607.1:c.20T=	ENSP00000419244.1:p.Phe7=
ENST00000562308.5:c.27T=
ENST00000565169.1:c.85T=
ENST00000569170.5:c.85T=
NM_001195794.1:c.356T= , LRG_700t1:c.356T=	NP_001182723.1:p.Phe119=
NM_001256819.1:c.528T=	NP_001243748.1:p.Leu176=
NM_052995.2:c.128T= , LRG_700t2:c.128T=	NP_443721.1:p.Phe43=
NM_174878.2:c.356T=	NP_777367.1:p.Phe119=
NR_046380.2:n.798T=
XR_924167.1:n.668T=
NM_001256819.2:c.528T=	NP_001243748.1:p.Leu176=
NM_174878.3:c.356T= MANE Select	NP_777367.1:p.Phe119=
NR_046380.3:n.526T=