Canonical Allele Identifier: CA354955398

Gene: CLRN1

Linked Data

• MyVariant Identifiers: chr3:g.150659396C>G (hg19) ; chr3:g.150941609C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.150941609C>G , CM000665.2:g.150941609C>G	GRCh38
NC_000003.11:g.150659396C>G , CM000665.1:g.150659396C>G	GRCh37
NC_000003.10:g.152142086C>G	NCBI36
NG_009168.1:g.36391G>C , LRG_700:g.36391G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327047.6:c.406G>C MANE Select	ENSP00000322280.1:p.Gly136Arg
ENST00000468836.2:c.554G>C	ENSP00000419892.2:n.554G>C
ENST00000644099.1:c.398G>C	ENSP00000494762.1:n.398G>C
ENST00000295911.6:c.178G>C	ENSP00000295911.2:p.Gly60Arg
ENST00000327047.5:c.406G>C	ENSP00000322280.1:p.Gly136Arg
ENST00000328863.8:c.406G>C	ENSP00000329158.4:p.Gly136Arg
ENST00000468836.1:c.178G>C	ENSP00000419892.1:p.Gly60Arg
ENST00000472224.1:n.412G>C
ENST00000485607.1:c.70G>C	ENSP00000419244.1:p.Gly24Arg
ENST00000562308.5:c.77G>C
ENST00000565169.1:c.135G>C
ENST00000569170.5:c.135G>C
NM_001195794.1:c.406G>C , LRG_700t1:c.406G>C	NP_001182723.1:p.Gly136Arg
NM_001256819.1:c.*20G>C	NP_001243748.1:n.*20G>C
NM_052995.2:c.178G>C , LRG_700t2:c.178G>C	NP_443721.1:p.Gly60Arg
NM_174878.2:c.406G>C	NP_777367.1:p.Gly136Arg
NR_046380.2:n.848G>C
XR_924167.1:n.718G>C
NM_001256819.2:c.*20G>C	NP_001243748.1:n.*20G>C
NM_174878.3:c.406G>C MANE Select	NP_777367.1:p.Gly136Arg
NR_046380.3:n.576G>C