Canonical Allele Identifier: CA1410910153
Gene: CLRN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.150972396C= , CM000665.2:g.150972396C= GRCh38
NC_000003.11:g.150690183C= , CM000665.1:g.150690183C= GRCh37
NC_000003.10:g.152172873C= NCBI36
NG_009168.1:g.5604G= , LRG_700:g.5604G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000327047.6:c.253+60G= MANE Select ENSP00000322280.1:n.253+60G=
ENST00000468836.2:c.229+60G= ENSP00000419892.2:n.229+60G=
ENST00000644099.1:c.94+60G= ENSP00000494762.1:n.94+60G=
ENST00000645441.1:c.95+60G=
ENST00000327047.5:c.253+60G= ENSP00000322280.1:n.253+60G=
ENST00000328863.8:c.253+60G= ENSP00000329158.4:n.253+60G=
ENST00000468836.1:c.-148+60G= ENSP00000419892.1:n.-148+60G=
ENST00000472224.1:n.259+60G=
NM_001195794.1:c.253+60G= , LRG_700t1:c.253+60G= NP_001182723.1:n.253+60G=
NM_001256819.1:c.253+60G= NP_001243748.1:n.253+60G=
NM_174878.2:c.253+60G= NP_777367.1:n.253+60G=
NR_046380.2:n.544+60G=
XR_924167.1:n.565+60G=
NM_001256819.2:c.253+60G= NP_001243748.1:n.253+60G=
NM_174878.3:c.253+60G= MANE Select NP_777367.1:n.253+60G=
NR_046380.3:n.272+60G=