Canonical Allele Identifier: CA1410910227
Gene: CLRN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.150972535C= , CM000665.2:g.150972535C= GRCh38
NC_000003.11:g.150690322C= , CM000665.1:g.150690322C= GRCh37
NC_000003.10:g.152173012C= NCBI36
NG_009168.1:g.5465G= , LRG_700:g.5465G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000327047.6:c.174G= MANE Select ENSP00000322280.1:p.Met58=
ENST00000468836.2:c.150G= ENSP00000419892.2:p.Met50=
ENST00000644099.1:c.15G= ENSP00000494762.1:p.Met5=
ENST00000645441.1:c.16G=
ENST00000327047.5:c.174G= ENSP00000322280.1:p.Met58=
ENST00000328863.8:c.174G= ENSP00000329158.4:p.Met58=
ENST00000468836.1:c.-227G= ENSP00000419892.1:n.-227G=
ENST00000472224.1:n.180G=
NM_001195794.1:c.174G= , LRG_700t1:c.174G= NP_001182723.1:p.Met58=
NM_001256819.1:c.174G= NP_001243748.1:p.Met58=
NM_174878.2:c.174G= NP_777367.1:p.Met58=
NR_046380.2:n.465G=
XR_924167.1:n.486G=
NM_001256819.2:c.174G= NP_001243748.1:p.Met58=
NM_174878.3:c.174G= MANE Select NP_777367.1:p.Met58=
NR_046380.3:n.193G=