Canonical Allele Identifier: CA1410888503

Gene: CLRN1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.150941666C= , CM000665.2:g.150941666C=	GRCh38
NC_000003.11:g.150659453C= , CM000665.1:g.150659453C=	GRCh37
NC_000003.10:g.152142143C=	NCBI36
NG_009168.1:g.36334G= , LRG_700:g.36334G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327047.6:c.349G= MANE Select	ENSP00000322280.1:p.Ala117=
ENST00000468836.2:c.497G=	ENSP00000419892.2:p.Ser166=
ENST00000644099.1:c.341G=	ENSP00000494762.1:n.341G=
ENST00000295911.6:c.121G=	ENSP00000295911.2:p.Ala41=
ENST00000327047.5:c.349G=	ENSP00000322280.1:p.Ala117=
ENST00000328863.8:c.349G=	ENSP00000329158.4:p.Ala117=
ENST00000468836.1:c.121G=	ENSP00000419892.1:p.Ala41=
ENST00000472224.1:n.355G=
ENST00000485607.1:c.13G=	ENSP00000419244.1:p.Ala5=
ENST00000562308.5:c.20G=
ENST00000565169.1:c.78G=
ENST00000569170.5:c.78G=
NM_001195794.1:c.349G= , LRG_700t1:c.349G=	NP_001182723.1:p.Ala117=
NM_001256819.1:c.521G=	NP_001243748.1:p.Ser174=
NM_052995.2:c.121G= , LRG_700t2:c.121G=	NP_443721.1:p.Ala41=
NM_174878.2:c.349G=	NP_777367.1:p.Ala117=
NR_046380.2:n.791G=
XR_924167.1:n.661G=
NM_001256819.2:c.521G=	NP_001243748.1:p.Ser174=
NM_174878.3:c.349G= MANE Select	NP_777367.1:p.Ala117=
NR_046380.3:n.519G=