Canonical Allele Identifier: CA1410883126
Gene: CLRN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.150927846T= , CM000665.2:g.150927846T= GRCh38
NC_000003.11:g.150645633T= , CM000665.1:g.150645633T= GRCh37
NC_000003.10:g.152128323T= NCBI36
NG_009168.1:g.50154A= , LRG_700:g.50154A=

Transcript Alleles

HGVS Amino-acid change
ENST00000327047.6:c.*90A= MANE Select ENSP00000322280.1:n.*90A=
ENST00000295911.6:c.342+219A= ENSP00000295911.2:n.342+219A=
ENST00000327047.5:c.*90A= ENSP00000322280.1:n.*90A=
ENST00000562308.5:c.104+13736A=
ENST00000565169.1:c.162+13736A=
ENST00000569170.5:c.162+13736A=
NM_001195794.1:c.*90A= , LRG_700t1:c.*90A= NP_001182723.1:n.*90A=
NM_001256819.1:c.*403A= NP_001243748.1:n.*403A=
NM_052995.2:c.342+219A= , LRG_700t2:c.342+219A= NP_443721.1:n.342+219A=
NM_174878.2:c.*90A= NP_777367.1:n.*90A=
NR_046380.2:n.1270A=
XR_924167.1:n.1101A=
NM_001256819.2:c.*403A= NP_001243748.1:n.*403A=
NM_174878.3:c.*90A= MANE Select NP_777367.1:n.*90A=
NR_046380.3:n.998A=