Canonical Allele Identifier: CA354955837

Gene: CLRN1

Linked Data

• MyVariant Identifiers: chr3:g.150659482A>T (hg19) ; chr3:g.150941695A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.150941695A>T , CM000665.2:g.150941695A>T	GRCh38
NC_000003.11:g.150659482A>T , CM000665.1:g.150659482A>T	GRCh37
NC_000003.10:g.152142172A>T	NCBI36
NG_009168.1:g.36305T>A , LRG_700:g.36305T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327047.6:c.320T>A MANE Select	ENSP00000322280.1:p.Ile107Asn
ENST00000468836.2:c.468T>A	ENSP00000419892.2:p.His156Gln
ENST00000644099.1:c.312T>A	ENSP00000494762.1:n.312T>A
ENST00000295911.6:c.92T>A	ENSP00000295911.2:p.Ile31Asn
ENST00000327047.5:c.320T>A	ENSP00000322280.1:p.Ile107Asn
ENST00000328863.8:c.320T>A	ENSP00000329158.4:p.Ile107Asn
ENST00000468836.1:c.92T>A	ENSP00000419892.1:p.Ile31Asn
ENST00000472224.1:n.326T>A
ENST00000485607.1:c.-17T>A	ENSP00000419244.1:n.-17T>A
ENST00000565169.1:c.49T>A
ENST00000569170.5:c.49T>A
NM_001195794.1:c.320T>A , LRG_700t1:c.320T>A	NP_001182723.1:p.Ile107Asn
NM_001256819.1:c.492T>A	NP_001243748.1:p.His164Gln
NM_052995.2:c.92T>A , LRG_700t2:c.92T>A	NP_443721.1:p.Ile31Asn
NM_174878.2:c.320T>A	NP_777367.1:p.Ile107Asn
NR_046380.2:n.762T>A
XR_924167.1:n.632T>A
NM_001256819.2:c.492T>A	NP_001243748.1:p.His164Gln
NM_174878.3:c.320T>A MANE Select	NP_777367.1:p.Ile107Asn
NR_046380.3:n.490T>A