Canonical Allele Identifier: CA354955355

Gene: CLRN1

Linked Data

• MyVariant Identifiers: chr3:g.150659387G>T (hg19) ; chr3:g.150941600G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.150941600G>T , CM000665.2:g.150941600G>T	GRCh38
NC_000003.11:g.150659387G>T , CM000665.1:g.150659387G>T	GRCh37
NC_000003.10:g.152142077G>T	NCBI36
NG_009168.1:g.36400C>A , LRG_700:g.36400C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327047.6:c.415C>A MANE Select	ENSP00000322280.1:p.Leu139Ile
ENST00000468836.2:c.563C>A	ENSP00000419892.2:n.563C>A
ENST00000644099.1:c.407C>A	ENSP00000494762.1:n.407C>A
ENST00000295911.6:c.187C>A	ENSP00000295911.2:p.Leu63Ile
ENST00000327047.5:c.415C>A	ENSP00000322280.1:p.Leu139Ile
ENST00000328863.8:c.415C>A	ENSP00000329158.4:p.Leu139Ile
ENST00000468836.1:c.187C>A	ENSP00000419892.1:p.Leu63Ile
ENST00000472224.1:n.421C>A
ENST00000485607.1:c.79C>A	ENSP00000419244.1:p.Leu27Ile
ENST00000562308.5:c.86C>A
ENST00000565169.1:c.144C>A
ENST00000569170.5:c.144C>A
NM_001195794.1:c.415C>A , LRG_700t1:c.415C>A	NP_001182723.1:p.Leu139Ile
NM_001256819.1:c.*29C>A	NP_001243748.1:n.*29C>A
NM_052995.2:c.187C>A , LRG_700t2:c.187C>A	NP_443721.1:p.Leu63Ile
NM_174878.2:c.415C>A	NP_777367.1:p.Leu139Ile
NR_046380.2:n.857C>A
XR_924167.1:n.727C>A
NM_001256819.2:c.*29C>A	NP_001243748.1:n.*29C>A
NM_174878.3:c.415C>A MANE Select	NP_777367.1:p.Leu139Ile
NR_046380.3:n.585C>A