Canonical Allele Identifier: CA1410910262
Gene: CLRN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.150972591A= , CM000665.2:g.150972591A= GRCh38
NC_000003.11:g.150690378A= , CM000665.1:g.150690378A= GRCh37
NC_000003.10:g.152173068A= NCBI36
NG_009168.1:g.5409T= , LRG_700:g.5409T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000327047.6:c.118T= MANE Select ENSP00000322280.1:p.Cys40=
ENST00000468836.2:c.94T= ENSP00000419892.2:p.Cys32=
ENST00000327047.5:c.118T= ENSP00000322280.1:p.Cys40=
ENST00000328863.8:c.118T= ENSP00000329158.4:p.Cys40=
ENST00000468836.1:c.-283T= ENSP00000419892.1:n.-283T=
ENST00000472224.1:n.124T=
NM_001195794.1:c.118T= , LRG_700t1:c.118T= NP_001182723.1:p.Cys40=
NM_001256819.1:c.118T= NP_001243748.1:p.Cys40=
NM_174878.2:c.118T= NP_777367.1:p.Cys40=
NR_046380.2:n.409T=
XR_924167.1:n.430T=
NM_001256819.2:c.118T= NP_001243748.1:p.Cys40=
NM_174878.3:c.118T= MANE Select NP_777367.1:p.Cys40=
NR_046380.3:n.137T=