Canonical Allele Identifier: CA354956017

Gene: CLRN1

Linked Data

• MyVariant Identifiers: chr3:g.150659510G>C (hg19) ; chr3:g.150941723G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.150941723G>C , CM000665.2:g.150941723G>C	GRCh38
NC_000003.11:g.150659510G>C , CM000665.1:g.150659510G>C	GRCh37
NC_000003.10:g.152142200G>C	NCBI36
NG_009168.1:g.36277C>G , LRG_700:g.36277C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327047.6:c.292C>G MANE Select	ENSP00000322280.1:p.His98Asp
ENST00000468836.2:c.440C>G	ENSP00000419892.2:p.Pro147Arg
ENST00000644099.1:c.284C>G	ENSP00000494762.1:n.284C>G
ENST00000295911.6:c.64C>G	ENSP00000295911.2:p.His22Asp
ENST00000327047.5:c.292C>G	ENSP00000322280.1:p.His98Asp
ENST00000328863.8:c.292C>G	ENSP00000329158.4:p.His98Asp
ENST00000468836.1:c.64C>G	ENSP00000419892.1:p.His22Asp
ENST00000472224.1:n.298C>G
ENST00000485607.1:c.-45C>G	ENSP00000419244.1:n.-45C>G
ENST00000565169.1:c.21C>G
ENST00000569170.5:c.21C>G
NM_001195794.1:c.292C>G , LRG_700t1:c.292C>G	NP_001182723.1:p.His98Asp
NM_001256819.1:c.464C>G	NP_001243748.1:p.Pro155Arg
NM_052995.2:c.64C>G , LRG_700t2:c.64C>G	NP_443721.1:p.His22Asp
NM_174878.2:c.292C>G	NP_777367.1:p.His98Asp
NR_046380.2:n.734C>G
XR_924167.1:n.604C>G
NM_001256819.2:c.464C>G	NP_001243748.1:p.Pro155Arg
NM_174878.3:c.292C>G MANE Select	NP_777367.1:p.His98Asp
NR_046380.3:n.462C>G