Canonical Allele Identifier: CA1410910240
Gene: CLRN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.150972558C= , CM000665.2:g.150972558C= GRCh38
NC_000003.11:g.150690345C= , CM000665.1:g.150690345C= GRCh37
NC_000003.10:g.152173035C= NCBI36
NG_009168.1:g.5442G= , LRG_700:g.5442G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000327047.6:c.151G= MANE Select ENSP00000322280.1:p.Gly51=
ENST00000468836.2:c.127G= ENSP00000419892.2:p.Gly43=
ENST00000327047.5:c.151G= ENSP00000322280.1:p.Gly51=
ENST00000328863.8:c.151G= ENSP00000329158.4:p.Gly51=
ENST00000468836.1:c.-250G= ENSP00000419892.1:n.-250G=
ENST00000472224.1:n.157G=
NM_001195794.1:c.151G= , LRG_700t1:c.151G= NP_001182723.1:p.Gly51=
NM_001256819.1:c.151G= NP_001243748.1:p.Gly51=
NM_174878.2:c.151G= NP_777367.1:p.Gly51=
NR_046380.2:n.442G=
XR_924167.1:n.463G=
NM_001256819.2:c.151G= NP_001243748.1:p.Gly51=
NM_174878.3:c.151G= MANE Select NP_777367.1:p.Gly51=
NR_046380.3:n.170G=