Canonical Allele Identifier: CA1410887973

Gene: CLRN1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.150940691G= , CM000665.2:g.150940691G=	GRCh38
NC_000003.11:g.150658478G= , CM000665.1:g.150658478G=	GRCh37
NC_000003.10:g.152141168G=	NCBI36
NG_009168.1:g.37309C= , LRG_700:g.37309C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327047.6:c.433+891C= MANE Select	ENSP00000322280.1:n.433+891C=
ENST00000468836.2:c.581+891C=	ENSP00000419892.2:n.581+891C=
ENST00000644099.1:c.426-172C=	ENSP00000494762.1:n.426-172C=
ENST00000295911.6:c.205+891C=	ENSP00000295911.2:n.205+891C=
ENST00000327047.5:c.433+891C=	ENSP00000322280.1:n.433+891C=
ENST00000328863.8:c.434-172C=	ENSP00000329158.4:n.434-172C=
ENST00000468836.1:c.205+891C=	ENSP00000419892.1:n.205+891C=
ENST00000485607.1:c.97+891C=	ENSP00000419244.1:n.97+891C=
ENST00000562308.5:c.104+891C=
ENST00000565169.1:c.162+891C=
ENST00000569170.5:c.162+891C=
NM_001195794.1:c.434-172C= , LRG_700t1:c.434-172C=	NP_001182723.1:n.434-172C=
NM_001256819.1:c.*47+891C=	NP_001243748.1:n.*47+891C=
NM_052995.2:c.205+891C= , LRG_700t2:c.205+891C=	NP_443721.1:n.205+891C=
NM_174878.2:c.433+891C=	NP_777367.1:n.433+891C=
NR_046380.2:n.876-172C=
XR_924167.1:n.745+891C=
NM_001256819.2:c.*47+891C=	NP_001243748.1:n.*47+891C=
NM_174878.3:c.433+891C= MANE Select	NP_777367.1:n.433+891C=
NR_046380.3:n.604-172C=