Canonical Allele Identifier: CA1410888529

Gene: CLRN1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.150941718G= , CM000665.2:g.150941718G=	GRCh38
NC_000003.11:g.150659505G= , CM000665.1:g.150659505G=	GRCh37
NC_000003.10:g.152142195G=	NCBI36
NG_009168.1:g.36282C= , LRG_700:g.36282C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327047.6:c.297C= MANE Select	ENSP00000322280.1:p.Val99=
ENST00000468836.2:c.445C=	ENSP00000419892.2:p.Gln149=
ENST00000644099.1:c.289C=	ENSP00000494762.1:n.289C=
ENST00000295911.6:c.69C=	ENSP00000295911.2:p.Val23=
ENST00000327047.5:c.297C=	ENSP00000322280.1:p.Val99=
ENST00000328863.8:c.297C=	ENSP00000329158.4:p.Val99=
ENST00000468836.1:c.69C=	ENSP00000419892.1:p.Val23=
ENST00000472224.1:n.303C=
ENST00000485607.1:c.-40C=	ENSP00000419244.1:n.-40C=
ENST00000565169.1:c.26C=
ENST00000569170.5:c.26C=
NM_001195794.1:c.297C= , LRG_700t1:c.297C=	NP_001182723.1:p.Val99=
NM_001256819.1:c.469C=	NP_001243748.1:p.Gln157=
NM_052995.2:c.69C= , LRG_700t2:c.69C=	NP_443721.1:p.Val23=
NM_174878.2:c.297C=	NP_777367.1:p.Val99=
NR_046380.2:n.739C=
XR_924167.1:n.609C=
NM_001256819.2:c.469C=	NP_001243748.1:p.Gln157=
NM_174878.3:c.297C= MANE Select	NP_777367.1:p.Val99=
NR_046380.3:n.467C=