Canonical Allele Identifier: CA1410910245
Gene: CLRN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.150972564C= , CM000665.2:g.150972564C= GRCh38
NC_000003.11:g.150690351C= , CM000665.1:g.150690351C= GRCh37
NC_000003.10:g.152173041C= NCBI36
NG_009168.1:g.5436G= , LRG_700:g.5436G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000327047.6:c.145G= MANE Select ENSP00000322280.1:p.Ala49=
ENST00000468836.2:c.121G= ENSP00000419892.2:p.Ala41=
ENST00000327047.5:c.145G= ENSP00000322280.1:p.Ala49=
ENST00000328863.8:c.145G= ENSP00000329158.4:p.Ala49=
ENST00000468836.1:c.-256G= ENSP00000419892.1:n.-256G=
ENST00000472224.1:n.151G=
NM_001195794.1:c.145G= , LRG_700t1:c.145G= NP_001182723.1:p.Ala49=
NM_001256819.1:c.145G= NP_001243748.1:p.Ala49=
NM_174878.2:c.145G= NP_777367.1:p.Ala49=
NR_046380.2:n.436G=
XR_924167.1:n.457G=
NM_001256819.2:c.145G= NP_001243748.1:p.Ala49=
NM_174878.3:c.145G= MANE Select NP_777367.1:p.Ala49=
NR_046380.3:n.164G=