Canonical Allele Identifier: CA1410910188
Gene: CLRN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.150972459A= , CM000665.2:g.150972459A= GRCh38
NC_000003.11:g.150690246A= , CM000665.1:g.150690246A= GRCh37
NC_000003.10:g.152172936A= NCBI36
NG_009168.1:g.5541T= , LRG_700:g.5541T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000327047.6:c.250T= MANE Select ENSP00000322280.1:p.Ser84=
ENST00000468836.2:c.226T= ENSP00000419892.2:p.Ser76=
ENST00000644099.1:c.91T= ENSP00000494762.1:p.Ser31=
ENST00000645441.1:c.92T=
ENST00000327047.5:c.250T= ENSP00000322280.1:p.Ser84=
ENST00000328863.8:c.250T= ENSP00000329158.4:p.Ser84=
ENST00000468836.1:c.-151T= ENSP00000419892.1:n.-151T=
ENST00000472224.1:n.256T=
NM_001195794.1:c.250T= , LRG_700t1:c.250T= NP_001182723.1:p.Ser84=
NM_001256819.1:c.250T= NP_001243748.1:p.Ser84=
NM_174878.2:c.250T= NP_777367.1:p.Ser84=
NR_046380.2:n.541T=
XR_924167.1:n.562T=
NM_001256819.2:c.250T= NP_001243748.1:p.Ser84=
NM_174878.3:c.250T= MANE Select NP_777367.1:p.Ser84=
NR_046380.3:n.269T=