Canonical Allele Identifier: CA1410888502

Gene: CLRN1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.150941665G= , CM000665.2:g.150941665G=	GRCh38
NC_000003.11:g.150659452G= , CM000665.1:g.150659452G=	GRCh37
NC_000003.10:g.152142142G=	NCBI36
NG_009168.1:g.36335C= , LRG_700:g.36335C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327047.6:c.350C= MANE Select	ENSP00000322280.1:p.Ala117=
ENST00000468836.2:c.498C=	ENSP00000419892.2:p.Ser166=
ENST00000644099.1:c.342C=	ENSP00000494762.1:n.342C=
ENST00000295911.6:c.122C=	ENSP00000295911.2:p.Ala41=
ENST00000327047.5:c.350C=	ENSP00000322280.1:p.Ala117=
ENST00000328863.8:c.350C=	ENSP00000329158.4:p.Ala117=
ENST00000468836.1:c.122C=	ENSP00000419892.1:p.Ala41=
ENST00000472224.1:n.356C=
ENST00000485607.1:c.14C=	ENSP00000419244.1:p.Ala5=
ENST00000562308.5:c.21C=
ENST00000565169.1:c.79C=
ENST00000569170.5:c.79C=
NM_001195794.1:c.350C= , LRG_700t1:c.350C=	NP_001182723.1:p.Ala117=
NM_001256819.1:c.522C=	NP_001243748.1:p.Ser174=
NM_052995.2:c.122C= , LRG_700t2:c.122C=	NP_443721.1:p.Ala41=
NM_174878.2:c.350C=	NP_777367.1:p.Ala117=
NR_046380.2:n.792C=
XR_924167.1:n.662C=
NM_001256819.2:c.522C=	NP_001243748.1:p.Ser174=
NM_174878.3:c.350C= MANE Select	NP_777367.1:p.Ala117=
NR_046380.3:n.520C=