Canonical Allele Identifier: CA2668197829

Gene: CLRN1

Linked Data

• gnomAD v4: 3-150941569-A-AT

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.150941573dup , CM000665.2:g.150941573dup	GRCh38
NC_000003.11:g.150659360dup , CM000665.1:g.150659360dup	GRCh37
NC_000003.10:g.152142050dup	NCBI36
NG_009168.1:g.36430dup , LRG_700:g.36430dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327047.6:c.433+12dup MANE Select	ENSP00000322280.1:n.433+12dup
ENST00000468836.2:c.581+12dup	ENSP00000419892.2:n.581+12dup
ENST00000644099.1:c.425+12dup	ENSP00000494762.1:n.425+12dup
ENST00000295911.6:c.205+12dup	ENSP00000295911.2:n.205+12dup
ENST00000327047.5:c.433+12dup	ENSP00000322280.1:n.433+12dup
ENST00000328863.8:c.433+12dup	ENSP00000329158.4:n.433+12dup
ENST00000468836.1:c.205+12dup	ENSP00000419892.1:n.205+12dup
ENST00000472224.1:n.451dup
ENST00000485607.1:c.97+12dup	ENSP00000419244.1:n.97+12dup
ENST00000562308.5:c.104+12dup
ENST00000565169.1:c.162+12dup
ENST00000569170.5:c.162+12dup
NM_001195794.1:c.433+12dup , LRG_700t1:c.433+12dup	NP_001182723.1:n.433+12dup
NM_001256819.1:c.*47+12dup	NP_001243748.1:n.*47+12dup
NM_052995.2:c.205+12dup , LRG_700t2:c.205+12dup	NP_443721.1:n.205+12dup
NM_174878.2:c.433+12dup	NP_777367.1:n.433+12dup
NR_046380.2:n.875+12dup
XR_924167.1:n.745+12dup
NM_001256819.2:c.*47+12dup	NP_001243748.1:n.*47+12dup
NM_174878.3:c.433+12dup MANE Select	NP_777367.1:n.433+12dup
NR_046380.3:n.603+12dup