Canonical Allele Identifier: CA1410910268
Gene: CLRN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.150972607G= , CM000665.2:g.150972607G= GRCh38
NC_000003.11:g.150690394G= , CM000665.1:g.150690394G= GRCh37
NC_000003.10:g.152173084G= NCBI36
NG_009168.1:g.5393C= , LRG_700:g.5393C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000327047.6:c.102C= MANE Select ENSP00000322280.1:p.Ile34=
ENST00000468836.2:c.78C= ENSP00000419892.2:p.Ile26=
ENST00000327047.5:c.102C= ENSP00000322280.1:p.Ile34=
ENST00000328863.8:c.102C= ENSP00000329158.4:p.Ile34=
ENST00000468836.1:c.-299C= ENSP00000419892.1:n.-299C=
ENST00000472224.1:n.108C=
NM_001195794.1:c.102C= , LRG_700t1:c.102C= NP_001182723.1:p.Ile34=
NM_001256819.1:c.102C= NP_001243748.1:p.Ile34=
NM_174878.2:c.102C= NP_777367.1:p.Ile34=
NR_046380.2:n.393C=
XR_924167.1:n.414C=
NM_001256819.2:c.102C= NP_001243748.1:p.Ile34=
NM_174878.3:c.102C= MANE Select NP_777367.1:p.Ile34=
NR_046380.3:n.121C=