Canonical Allele Identifier: CA1410888507

Gene: CLRN1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.150941672C= , CM000665.2:g.150941672C=	GRCh38
NC_000003.11:g.150659459C= , CM000665.1:g.150659459C=	GRCh37
NC_000003.10:g.152142149C=	NCBI36
NG_009168.1:g.36328G= , LRG_700:g.36328G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327047.6:c.343G= MANE Select	ENSP00000322280.1:p.Gly115=
ENST00000468836.2:c.491G=	ENSP00000419892.2:p.Gly164=
ENST00000644099.1:c.335G=	ENSP00000494762.1:n.335G=
ENST00000295911.6:c.115G=	ENSP00000295911.2:p.Gly39=
ENST00000327047.5:c.343G=	ENSP00000322280.1:p.Gly115=
ENST00000328863.8:c.343G=	ENSP00000329158.4:p.Gly115=
ENST00000468836.1:c.115G=	ENSP00000419892.1:p.Gly39=
ENST00000472224.1:n.349G=
ENST00000485607.1:c.7G=	ENSP00000419244.1:p.Gly3=
ENST00000562308.5:c.14G=
ENST00000565169.1:c.72G=
ENST00000569170.5:c.72G=
NM_001195794.1:c.343G= , LRG_700t1:c.343G=	NP_001182723.1:p.Gly115=
NM_001256819.1:c.515G=	NP_001243748.1:p.Gly172=
NM_052995.2:c.115G= , LRG_700t2:c.115G=	NP_443721.1:p.Gly39=
NM_174878.2:c.343G=	NP_777367.1:p.Gly115=
NR_046380.2:n.785G=
XR_924167.1:n.655G=
NM_001256819.2:c.515G=	NP_001243748.1:p.Gly172=
NM_174878.3:c.343G= MANE Select	NP_777367.1:p.Gly115=
NR_046380.3:n.513G=