Canonical Allele Identifier: CA1410888498

Gene: CLRN1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.150941656A= , CM000665.2:g.150941656A=	GRCh38
NC_000003.11:g.150659443A= , CM000665.1:g.150659443A=	GRCh37
NC_000003.10:g.152142133A=	NCBI36
NG_009168.1:g.36344T= , LRG_700:g.36344T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327047.6:c.359T= MANE Select	ENSP00000322280.1:p.Met120=
ENST00000468836.2:c.507T=	ENSP00000419892.2:p.His169=
ENST00000644099.1:c.351T=	ENSP00000494762.1:n.351T=
ENST00000295911.6:c.131T=	ENSP00000295911.2:p.Met44=
ENST00000327047.5:c.359T=	ENSP00000322280.1:p.Met120=
ENST00000328863.8:c.359T=	ENSP00000329158.4:p.Met120=
ENST00000468836.1:c.131T=	ENSP00000419892.1:p.Met44=
ENST00000472224.1:n.365T=
ENST00000485607.1:c.23T=	ENSP00000419244.1:p.Met8=
ENST00000562308.5:c.30T=
ENST00000565169.1:c.88T=
ENST00000569170.5:c.88T=
NM_001195794.1:c.359T= , LRG_700t1:c.359T=	NP_001182723.1:p.Met120=
NM_001256819.1:c.531T=	NP_001243748.1:p.His177=
NM_052995.2:c.131T= , LRG_700t2:c.131T=	NP_443721.1:p.Met44=
NM_174878.2:c.359T=	NP_777367.1:p.Met120=
NR_046380.2:n.801T=
XR_924167.1:n.671T=
NM_001256819.2:c.531T=	NP_001243748.1:p.His177=
NM_174878.3:c.359T= MANE Select	NP_777367.1:p.Met120=
NR_046380.3:n.529T=