Canonical Allele Identifier: CA354956030

Gene: CLRN1

Linked Data

• MyVariant Identifiers: chr3:g.150659516T>C (hg19) ; chr3:g.150941729T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.150941729T>C , CM000665.2:g.150941729T>C	GRCh38
NC_000003.11:g.150659516T>C , CM000665.1:g.150659516T>C	GRCh37
NC_000003.10:g.152142206T>C	NCBI36
NG_009168.1:g.36271A>G , LRG_700:g.36271A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327047.6:c.286A>G MANE Select	ENSP00000322280.1:p.Ser96Gly
ENST00000468836.2:c.434A>G	ENSP00000419892.2:p.Glu145Gly
ENST00000644099.1:c.278A>G	ENSP00000494762.1:n.278A>G
ENST00000295911.6:c.58A>G	ENSP00000295911.2:p.Ser20Gly
ENST00000327047.5:c.286A>G	ENSP00000322280.1:p.Ser96Gly
ENST00000328863.8:c.286A>G	ENSP00000329158.4:p.Ser96Gly
ENST00000468836.1:c.58A>G	ENSP00000419892.1:p.Ser20Gly
ENST00000472224.1:n.292A>G
ENST00000485607.1:c.-51A>G	ENSP00000419244.1:n.-51A>G
ENST00000565169.1:c.15A>G
ENST00000569170.5:c.15A>G
NM_001195794.1:c.286A>G , LRG_700t1:c.286A>G	NP_001182723.1:p.Ser96Gly
NM_001256819.1:c.458A>G	NP_001243748.1:p.Glu153Gly
NM_052995.2:c.58A>G , LRG_700t2:c.58A>G	NP_443721.1:p.Ser20Gly
NM_174878.2:c.286A>G	NP_777367.1:p.Ser96Gly
NR_046380.2:n.728A>G
XR_924167.1:n.598A>G
NM_001256819.2:c.458A>G	NP_001243748.1:p.Glu153Gly
NM_174878.3:c.286A>G MANE Select	NP_777367.1:p.Ser96Gly
NR_046380.3:n.456A>G