Canonical Allele Identifier: CA1410910176

Gene: CLRN1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.150972438A= , CM000665.2:g.150972438A=	GRCh38
NC_000003.11:g.150690225A= , CM000665.1:g.150690225A=	GRCh37
NC_000003.10:g.152172915A=	NCBI36
NG_009168.1:g.5562T= , LRG_700:g.5562T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327047.6:c.253+18T= MANE Select	ENSP00000322280.1:n.253+18T=
ENST00000468836.2:c.229+18T=	ENSP00000419892.2:n.229+18T=
ENST00000644099.1:c.94+18T=	ENSP00000494762.1:n.94+18T=
ENST00000645441.1:c.95+18T=
ENST00000327047.5:c.253+18T=	ENSP00000322280.1:n.253+18T=
ENST00000328863.8:c.253+18T=	ENSP00000329158.4:n.253+18T=
ENST00000468836.1:c.-148+18T=	ENSP00000419892.1:n.-148+18T=
ENST00000472224.1:n.259+18T=
NM_001195794.1:c.253+18T= , LRG_700t1:c.253+18T=	NP_001182723.1:n.253+18T=
NM_001256819.1:c.253+18T=	NP_001243748.1:n.253+18T=
NM_174878.2:c.253+18T=	NP_777367.1:n.253+18T=
NR_046380.2:n.544+18T=
XR_924167.1:n.565+18T=
NM_001256819.2:c.253+18T=	NP_001243748.1:n.253+18T=
NM_174878.3:c.253+18T= MANE Select	NP_777367.1:n.253+18T=
NR_046380.3:n.272+18T=