Canonical Allele Identifier: CA1410882610

Gene: CLRN1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.150926681A= , CM000665.2:g.150926681A=	GRCh38
NC_000003.11:g.150644468A= , CM000665.1:g.150644468A=	GRCh37
NC_000003.10:g.152127158A=	NCBI36
NG_009168.1:g.51319T= , LRG_700:g.51319T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000327047.6:c.*1255T= MANE Select	ENSP00000322280.1:n.*1255T=
ENST00000295911.6:c.*171T=	ENSP00000295911.2:n.*171T=
ENST00000327047.5:c.*1255T=	ENSP00000322280.1:n.*1255T=
ENST00000562308.5:c.104+14901T=
ENST00000565169.1:c.162+14901T=
ENST00000569170.5:c.162+14901T=
NM_001195794.1:c.*1255T= , LRG_700t1:c.*1255T=	NP_001182723.1:n.*1255T=
NM_001256819.1:c.*1568T=	NP_001243748.1:n.*1568T=
NM_052995.2:c.*171T= , LRG_700t2:c.*171T=	NP_443721.1:n.*171T=
NM_174878.2:c.*1255T=	NP_777367.1:n.*1255T=
NR_046380.2:n.2435T=
XR_924167.1:n.2266T=
NM_001256819.2:c.*1568T=	NP_001243748.1:n.*1568T=
NM_174878.3:c.*1255T= MANE Select	NP_777367.1:n.*1255T=
NR_046380.3:n.2163T=