Canonical Allele Identifier: CA2758898385
Gene: CLRN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.150941875_150941876insACG , CM000665.2:g.150941875_150941876insACG GRCh38
NC_000003.11:g.150659662_150659663insACG , CM000665.1:g.150659662_150659663insACG GRCh37
NC_000003.10:g.152142352_152142353insACG NCBI36
NG_009168.1:g.36124_36125insCGT , LRG_700:g.36124_36125insCGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000327047.6:c.254-115_254-114insCGT MANE Select ENSP00000322280.1:n.254-115_254-114insCGT
ENST00000468836.2:c.402-115_402-114insCGT ENSP00000419892.2:n.402-115_402-114insCGT
ENST00000644099.1:c.246-115_246-114insCGT ENSP00000494762.1:n.246-115_246-114insCGT
ENST00000295911.6:c.26-115_26-114insCGT ENSP00000295911.2:n.26-115_26-114insCGT
ENST00000327047.5:c.254-115_254-114insCGT ENSP00000322280.1:n.254-115_254-114insCGT
ENST00000328863.8:c.254-115_254-114insCGT ENSP00000329158.4:n.254-115_254-114insCGT
ENST00000468836.1:c.26-115_26-114insCGT ENSP00000419892.1:n.26-115_26-114insCGT
ENST00000472224.1:n.260-115_260-114insCGT
ENST00000485607.1:c.-83-115_-83-114insCGT ENSP00000419244.1:n.-83-115_-83-114insCGT
NM_001195794.1:c.254-115_254-114insCGT , LRG_700t1:c.254-115_254-114insCGT NP_001182723.1:n.254-115_254-114insCGT
NM_001256819.1:c.426-115_426-114insCGT NP_001243748.1:n.426-115_426-114insCGT
NM_052995.2:c.26-115_26-114insCGT , LRG_700t2:c.26-115_26-114insCGT NP_443721.1:n.26-115_26-114insCGT
NM_174878.2:c.254-115_254-114insCGT NP_777367.1:n.254-115_254-114insCGT
NR_046380.2:n.696-115_696-114insCGT
XR_924167.1:n.566-115_566-114insCGT
NM_001256819.2:c.426-115_426-114insCGT NP_001243748.1:n.426-115_426-114insCGT
NM_174878.3:c.254-115_254-114insCGT MANE Select NP_777367.1:n.254-115_254-114insCGT
NR_046380.3:n.424-115_424-114insCGT