Canonical Allele Identifier: CA2668198785

Gene: CLRN1

Linked Data

• gnomAD v4: 3-150972350-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.150972350A>C , CM000665.2:g.150972350A>C	GRCh38
NC_000003.11:g.150690137A>C , CM000665.1:g.150690137A>C	GRCh37
NC_000003.10:g.152172827A>C	NCBI36
NG_009168.1:g.5650T>G , LRG_700:g.5650T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327047.6:c.253+106T>G MANE Select	ENSP00000322280.1:n.253+106T>G
ENST00000468836.2:c.229+106T>G	ENSP00000419892.2:n.229+106T>G
ENST00000644099.1:c.94+106T>G	ENSP00000494762.1:n.94+106T>G
ENST00000645441.1:c.95+106T>G
ENST00000327047.5:c.253+106T>G	ENSP00000322280.1:n.253+106T>G
ENST00000328863.8:c.253+106T>G	ENSP00000329158.4:n.253+106T>G
ENST00000468836.1:c.-148+106T>G	ENSP00000419892.1:n.-148+106T>G
ENST00000472224.1:n.259+106T>G
NM_001195794.1:c.253+106T>G , LRG_700t1:c.253+106T>G	NP_001182723.1:n.253+106T>G
NM_001256819.1:c.253+106T>G	NP_001243748.1:n.253+106T>G
NM_174878.2:c.253+106T>G	NP_777367.1:n.253+106T>G
NR_046380.2:n.544+106T>G
XR_924167.1:n.565+106T>G
NM_001256819.2:c.253+106T>G	NP_001243748.1:n.253+106T>G
NM_174878.3:c.253+106T>G MANE Select	NP_777367.1:n.253+106T>G
NR_046380.3:n.272+106T>G