Canonical Allele Identifier: CA1410910259
Gene: CLRN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.150972584G= , CM000665.2:g.150972584G= GRCh38
NC_000003.11:g.150690371G= , CM000665.1:g.150690371G= GRCh37
NC_000003.10:g.152173061G= NCBI36
NG_009168.1:g.5416C= , LRG_700:g.5416C=

Transcript Alleles

HGVS Amino-acid change
ENST00000327047.6:c.125C= MANE Select ENSP00000322280.1:p.Thr42=
ENST00000468836.2:c.101C= ENSP00000419892.2:p.Thr34=
ENST00000327047.5:c.125C= ENSP00000322280.1:p.Thr42=
ENST00000328863.8:c.125C= ENSP00000329158.4:p.Thr42=
ENST00000468836.1:c.-276C= ENSP00000419892.1:n.-276C=
ENST00000472224.1:n.131C=
NM_001195794.1:c.125C= , LRG_700t1:c.125C= NP_001182723.1:p.Thr42=
NM_001256819.1:c.125C= NP_001243748.1:p.Thr42=
NM_174878.2:c.125C= NP_777367.1:p.Thr42=
NR_046380.2:n.416C=
XR_924167.1:n.437C=
NM_001256819.2:c.125C= NP_001243748.1:p.Thr42=
NM_174878.3:c.125C= MANE Select NP_777367.1:p.Thr42=
NR_046380.3:n.144C=