Canonical Allele Identifier: CA1410887908
Gene: CLRN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.150940562_150940566delinsATTGT , CM000665.2:g.150940562_150940566delinsATTGT GRCh38
NC_000003.11:g.150658349_150658353delinsATTGT , CM000665.1:g.150658349_150658353delinsATTGT GRCh37
NC_000003.10:g.152141039_152141043delinsATTGT NCBI36
NG_009168.1:g.37434_37438delinsACAAT , LRG_700:g.37434_37438delinsACAAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000327047.6:c.433+1016_433+1020delinsACAAT MANE Select ENSP00000322280.1:n.433+1016_433+1020delinsACAAT
ENST00000468836.2:c.581+1016_581+1020delinsACAAT ENSP00000419892.2:n.581+1016_581+1020delinsACAAT
ENST00000644099.1:c.426-47_426-43delinsACAAT ENSP00000494762.1:n.426-47_426-43delinsACAAT
ENST00000295911.6:c.205+1016_205+1020delinsACAAT ENSP00000295911.2:n.205+1016_205+1020delinsACAAT
ENST00000327047.5:c.433+1016_433+1020delinsACAAT ENSP00000322280.1:n.433+1016_433+1020delinsACAAT
ENST00000328863.8:c.434-47_434-43delinsACAAT ENSP00000329158.4:n.434-47_434-43delinsACAAT
ENST00000468836.1:c.205+1016_205+1020delinsACAAT ENSP00000419892.1:n.205+1016_205+1020delinsACAAT
ENST00000485607.1:c.97+1016_97+1020delinsACAAT ENSP00000419244.1:n.97+1016_97+1020delinsACAAT
ENST00000562308.5:c.104+1016_104+1020delinsACAAT
ENST00000565169.1:c.162+1016_162+1020delinsACAAT
ENST00000569170.5:c.162+1016_162+1020delinsACAAT
NM_001195794.1:c.434-47_434-43delinsACAAT , LRG_700t1:c.434-47_434-43delinsACAAT NP_001182723.1:n.434-47_434-43delinsACAAT
NM_001256819.1:c.*47+1016_*47+1020delinsACAAT NP_001243748.1:n.*47+1016_*47+1020delinsACAAT
NM_052995.2:c.205+1016_205+1020delinsACAAT , LRG_700t2:c.205+1016_205+1020delinsACAAT NP_443721.1:n.205+1016_205+1020delinsACAAT
NM_174878.2:c.433+1016_433+1020delinsACAAT NP_777367.1:n.433+1016_433+1020delinsACAAT
NR_046380.2:n.876-47_876-43delinsACAAT
XR_924167.1:n.745+1016_745+1020delinsACAAT
NM_001256819.2:c.*47+1016_*47+1020delinsACAAT NP_001243748.1:n.*47+1016_*47+1020delinsACAAT
NM_174878.3:c.433+1016_433+1020delinsACAAT MANE Select NP_777367.1:n.433+1016_433+1020delinsACAAT
NR_046380.3:n.604-47_604-43delinsACAAT