Canonical Allele Identifier: CA2695199315
Community Standard Title: NM_174878.3(CLRN1):c.109dup (p.Thr37AsnfsTer24)
Gene: CLRN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.150972600dup , CM000665.2:g.150972600dup GRCh38
NC_000003.11:g.150690387dup , CM000665.1:g.150690387dup GRCh37
NC_000003.10:g.152173077dup NCBI36
NG_009168.1:g.5400dup , LRG_700:g.5400dup

Transcript Alleles

HGVS Amino-acid Change
NM_174878.3:c.109dup MANE Select NP_777367.1:p.Thr37AsnfsTer24
ENST00000327047.6:c.109dup MANE Select ENSP00000322280.1:p.Thr37AsnfsTer24
NM_001195794.1:c.109dup , LRG_700t1:c.109dup NP_001182723.1:p.Thr37AsnfsTer24
NM_001256819.1:c.109dup NP_001243748.1:p.Thr37AsnfsTer24
NM_001256819.2:c.109dup NP_001243748.1:p.Thr37AsnfsTer24
NM_174878.2:c.109dup NP_777367.1:p.Thr37AsnfsTer24
NR_046380.2:n.400dup
NR_046380.3:n.128dup
ENST00000327047.5:c.109dup ENSP00000322280.1:p.Thr37AsnfsTer24
ENST00000328863.8:c.109dup ENSP00000329158.4:p.Thr37AsnfsTer24
ENST00000468836.1:c.-292dup ENSP00000419892.1:n.-292dup
ENST00000468836.2:c.85dup ENSP00000419892.2:p.Thr29AsnfsTer24
ENST00000472224.1:n.115dup
XR_924167.1:n.421dup