Canonical Allele Identifier: CA1410882607

Gene: CLRN1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.150926671T= , CM000665.2:g.150926671T=	GRCh38
NC_000003.11:g.150644458T= , CM000665.1:g.150644458T=	GRCh37
NC_000003.10:g.152127148T=	NCBI36
NG_009168.1:g.51329A= , LRG_700:g.51329A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000327047.6:c.*1265A= MANE Select	ENSP00000322280.1:n.*1265A=
ENST00000295911.6:c.*181A=	ENSP00000295911.2:n.*181A=
ENST00000327047.5:c.*1265A=	ENSP00000322280.1:n.*1265A=
ENST00000562308.5:c.104+14911A=
ENST00000565169.1:c.162+14911A=
ENST00000569170.5:c.162+14911A=
NM_001195794.1:c.*1265A= , LRG_700t1:c.*1265A=	NP_001182723.1:n.*1265A=
NM_001256819.1:c.*1578A=	NP_001243748.1:n.*1578A=
NM_052995.2:c.*181A= , LRG_700t2:c.*181A=	NP_443721.1:n.*181A=
NM_174878.2:c.*1265A=	NP_777367.1:n.*1265A=
NR_046380.2:n.2445A=
XR_924167.1:n.2276A=
NM_001256819.2:c.*1578A=	NP_001243748.1:n.*1578A=
NM_174878.3:c.*1265A= MANE Select	NP_777367.1:n.*1265A=
NR_046380.3:n.2173A=