Canonical Allele Identifier: CA1410910284
Gene: CLRN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.150972640T= , CM000665.2:g.150972640T= GRCh38
NC_000003.11:g.150690427T= , CM000665.1:g.150690427T= GRCh37
NC_000003.10:g.152173117T= NCBI36
NG_009168.1:g.5360A= , LRG_700:g.5360A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000327047.6:c.69A= MANE Select ENSP00000322280.1:p.Gly23=
ENST00000468836.2:c.45A= ENSP00000419892.2:p.Gly15=
ENST00000327047.5:c.69A= ENSP00000322280.1:p.Gly23=
ENST00000328863.8:c.69A= ENSP00000329158.4:p.Gly23=
ENST00000468836.1:c.-332A= ENSP00000419892.1:n.-332A=
ENST00000472224.1:n.75A=
NM_001195794.1:c.69A= , LRG_700t1:c.69A= NP_001182723.1:p.Gly23=
NM_001256819.1:c.69A= NP_001243748.1:p.Gly23=
NM_174878.2:c.69A= NP_777367.1:p.Gly23=
NR_046380.2:n.360A=
XR_924167.1:n.381A=
NM_001256819.2:c.69A= NP_001243748.1:p.Gly23=
NM_174878.3:c.69A= MANE Select NP_777367.1:p.Gly23=
NR_046380.3:n.88A=