Canonical Allele Identifier: CA1410888531

Gene: CLRN1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.150941721G= , CM000665.2:g.150941721G=	GRCh38
NC_000003.11:g.150659508G= , CM000665.1:g.150659508G=	GRCh37
NC_000003.10:g.152142198G=	NCBI36
NG_009168.1:g.36279C= , LRG_700:g.36279C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327047.6:c.294C= MANE Select	ENSP00000322280.1:p.His98=
ENST00000468836.2:c.442C=	ENSP00000419892.2:p.Arg148=
ENST00000644099.1:c.286C=	ENSP00000494762.1:n.286C=
ENST00000295911.6:c.66C=	ENSP00000295911.2:p.His22=
ENST00000327047.5:c.294C=	ENSP00000322280.1:p.His98=
ENST00000328863.8:c.294C=	ENSP00000329158.4:p.His98=
ENST00000468836.1:c.66C=	ENSP00000419892.1:p.His22=
ENST00000472224.1:n.300C=
ENST00000485607.1:c.-43C=	ENSP00000419244.1:n.-43C=
ENST00000565169.1:c.23C=
ENST00000569170.5:c.23C=
NM_001195794.1:c.294C= , LRG_700t1:c.294C=	NP_001182723.1:p.His98=
NM_001256819.1:c.466C=	NP_001243748.1:p.Arg156=
NM_052995.2:c.66C= , LRG_700t2:c.66C=	NP_443721.1:p.His22=
NM_174878.2:c.294C=	NP_777367.1:p.His98=
NR_046380.2:n.736C=
XR_924167.1:n.606C=
NM_001256819.2:c.466C=	NP_001243748.1:p.Arg156=
NM_174878.3:c.294C= MANE Select	NP_777367.1:p.His98=
NR_046380.3:n.464C=