Canonical Allele Identifier: CA1410888650

Gene: CLRN1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.150941976G= , CM000665.2:g.150941976G=	GRCh38
NC_000003.11:g.150659763G= , CM000665.1:g.150659763G=	GRCh37
NC_000003.10:g.152142453G=	NCBI36
NG_009168.1:g.36024C= , LRG_700:g.36024C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327047.6:c.254-215C= MANE Select	ENSP00000322280.1:n.254-215C=
ENST00000468836.2:c.402-215C=	ENSP00000419892.2:n.402-215C=
ENST00000644099.1:c.246-215C=	ENSP00000494762.1:n.246-215C=
ENST00000295911.6:c.26-215C=	ENSP00000295911.2:n.26-215C=
ENST00000327047.5:c.254-215C=	ENSP00000322280.1:n.254-215C=
ENST00000328863.8:c.254-215C=	ENSP00000329158.4:n.254-215C=
ENST00000468836.1:c.26-215C=	ENSP00000419892.1:n.26-215C=
ENST00000472224.1:n.260-215C=
ENST00000485607.1:c.-83-215C=	ENSP00000419244.1:n.-83-215C=
NM_001195794.1:c.254-215C= , LRG_700t1:c.254-215C=	NP_001182723.1:n.254-215C=
NM_001256819.1:c.426-215C=	NP_001243748.1:n.426-215C=
NM_052995.2:c.26-215C= , LRG_700t2:c.26-215C=	NP_443721.1:n.26-215C=
NM_174878.2:c.254-215C=	NP_777367.1:n.254-215C=
NR_046380.2:n.696-215C=
XR_924167.1:n.566-215C=
NM_001256819.2:c.426-215C=	NP_001243748.1:n.426-215C=
NM_174878.3:c.254-215C= MANE Select	NP_777367.1:n.254-215C=
NR_046380.3:n.424-215C=