Canonical Allele Identifier: CA2668197808
Gene: CLRN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.150941525_150941526dup , CM000665.2:g.150941525_150941526dup GRCh38
NC_000003.11:g.150659312_150659313dup , CM000665.1:g.150659312_150659313dup GRCh37
NC_000003.10:g.152142002_152142003dup NCBI36
NG_009168.1:g.36474_36475dup , LRG_700:g.36474_36475dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000327047.6:c.433+56_433+57dup MANE Select ENSP00000322280.1:n.433+56_433+57dup
ENST00000468836.2:c.581+56_581+57dup ENSP00000419892.2:n.581+56_581+57dup
ENST00000644099.1:c.425+56_425+57dup ENSP00000494762.1:n.425+56_425+57dup
ENST00000295911.6:c.205+56_205+57dup ENSP00000295911.2:n.205+56_205+57dup
ENST00000327047.5:c.433+56_433+57dup ENSP00000322280.1:n.433+56_433+57dup
ENST00000328863.8:c.433+56_433+57dup ENSP00000329158.4:n.433+56_433+57dup
ENST00000468836.1:c.205+56_205+57dup ENSP00000419892.1:n.205+56_205+57dup
ENST00000472224.1:n.495_496dup
ENST00000485607.1:c.97+56_97+57dup ENSP00000419244.1:n.97+56_97+57dup
ENST00000562308.5:c.104+56_104+57dup
ENST00000565169.1:c.162+56_162+57dup
ENST00000569170.5:c.162+56_162+57dup
NM_001195794.1:c.433+56_433+57dup , LRG_700t1:c.433+56_433+57dup NP_001182723.1:n.433+56_433+57dup
NM_001256819.1:c.*47+56_*47+57dup NP_001243748.1:n.*47+56_*47+57dup
NM_052995.2:c.205+56_205+57dup , LRG_700t2:c.205+56_205+57dup NP_443721.1:n.205+56_205+57dup
NM_174878.2:c.433+56_433+57dup NP_777367.1:n.433+56_433+57dup
NR_046380.2:n.875+56_875+57dup
XR_924167.1:n.745+56_745+57dup
NM_001256819.2:c.*47+56_*47+57dup NP_001243748.1:n.*47+56_*47+57dup
NM_174878.3:c.433+56_433+57dup MANE Select NP_777367.1:n.433+56_433+57dup
NR_046380.3:n.603+56_603+57dup