Canonical Allele Identifier: CA1410888482

Gene: CLRN1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.150941617C= , CM000665.2:g.150941617C=	GRCh38
NC_000003.11:g.150659404C= , CM000665.1:g.150659404C=	GRCh37
NC_000003.10:g.152142094C=	NCBI36
NG_009168.1:g.36383G= , LRG_700:g.36383G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327047.6:c.398G= MANE Select	ENSP00000322280.1:p.Gly133=
ENST00000468836.2:c.546G=	ENSP00000419892.2:n.546G=
ENST00000644099.1:c.390G=	ENSP00000494762.1:n.390G=
ENST00000295911.6:c.170G=	ENSP00000295911.2:p.Gly57=
ENST00000327047.5:c.398G=	ENSP00000322280.1:p.Gly133=
ENST00000328863.8:c.398G=	ENSP00000329158.4:p.Gly133=
ENST00000468836.1:c.170G=	ENSP00000419892.1:p.Gly57=
ENST00000472224.1:n.404G=
ENST00000485607.1:c.62G=	ENSP00000419244.1:p.Gly21=
ENST00000562308.5:c.69G=
ENST00000565169.1:c.127G=
ENST00000569170.5:c.127G=
NM_001195794.1:c.398G= , LRG_700t1:c.398G=	NP_001182723.1:p.Gly133=
NM_001256819.1:c.*12G=	NP_001243748.1:n.*12G=
NM_052995.2:c.170G= , LRG_700t2:c.170G=	NP_443721.1:p.Gly57=
NM_174878.2:c.398G=	NP_777367.1:p.Gly133=
NR_046380.2:n.840G=
XR_924167.1:n.710G=
NM_001256819.2:c.*12G=	NP_001243748.1:n.*12G=
NM_174878.3:c.398G= MANE Select	NP_777367.1:p.Gly133=
NR_046380.3:n.568G=