Canonical Allele Identifier: CA436393842

Gene: CLRN1

Linked Data

• MyVariant Identifiers: chr3:g.150645756T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.150927969T>C , CM000665.2:g.150927969T>C	GRCh38
NC_000003.11:g.150645756T>C , CM000665.1:g.150645756T>C	GRCh37
NC_000003.10:g.152128446T>C	NCBI36
NG_009168.1:g.50031A>G , LRG_700:g.50031A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327047.6:c.666A>G MANE Select	ENSP00000322280.1:p.Glu222=
ENST00000295911.6:c.342+96A>G	ENSP00000295911.2:n.342+96A>G
ENST00000327047.5:c.666A>G	ENSP00000322280.1:p.Glu222=
ENST00000328863.8:c.705A>G	ENSP00000329158.4:p.Glu235=
ENST00000562308.5:c.104+13613A>G
ENST00000565169.1:c.162+13613A>G
ENST00000569170.5:c.162+13613A>G
NM_001195794.1:c.705A>G , LRG_700t1:c.705A>G	NP_001182723.1:p.Glu235=
NM_001256819.1:c.*280A>G	NP_001243748.1:n.*280A>G
NM_052995.2:c.342+96A>G , LRG_700t2:c.342+96A>G	NP_443721.1:n.342+96A>G
NM_174878.2:c.666A>G	NP_777367.1:p.Glu222=
NR_046380.2:n.1147A>G
XR_924167.1:n.978A>G
NM_001256819.2:c.*280A>G	NP_001243748.1:n.*280A>G
NM_174878.3:c.666A>G MANE Select	NP_777367.1:p.Glu222=
NR_046380.3:n.875A>G