Canonical Allele Identifier: CA1410910209
Gene: CLRN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.150972507C= , CM000665.2:g.150972507C= GRCh38
NC_000003.11:g.150690294C= , CM000665.1:g.150690294C= GRCh37
NC_000003.10:g.152172984C= NCBI36
NG_009168.1:g.5493G= , LRG_700:g.5493G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000327047.6:c.202G= MANE Select ENSP00000322280.1:p.Gly68=
ENST00000468836.2:c.178G= ENSP00000419892.2:p.Gly60=
ENST00000644099.1:c.43G= ENSP00000494762.1:p.Gly15=
ENST00000645441.1:c.44G=
ENST00000327047.5:c.202G= ENSP00000322280.1:p.Gly68=
ENST00000328863.8:c.202G= ENSP00000329158.4:p.Gly68=
ENST00000468836.1:c.-199G= ENSP00000419892.1:n.-199G=
ENST00000472224.1:n.208G=
NM_001195794.1:c.202G= , LRG_700t1:c.202G= NP_001182723.1:p.Gly68=
NM_001256819.1:c.202G= NP_001243748.1:p.Gly68=
NM_174878.2:c.202G= NP_777367.1:p.Gly68=
NR_046380.2:n.493G=
XR_924167.1:n.514G=
NM_001256819.2:c.202G= NP_001243748.1:p.Gly68=
NM_174878.3:c.202G= MANE Select NP_777367.1:p.Gly68=
NR_046380.3:n.221G=