Canonical Allele Identifier: CA354956007

Gene: CLRN1

Linked Data

• MyVariant Identifiers: chr3:g.150659507C>G (hg19) ; chr3:g.150941720C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.150941720C>G , CM000665.2:g.150941720C>G	GRCh38
NC_000003.11:g.150659507C>G , CM000665.1:g.150659507C>G	GRCh37
NC_000003.10:g.152142197C>G	NCBI36
NG_009168.1:g.36280G>C , LRG_700:g.36280G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327047.6:c.295G>C MANE Select	ENSP00000322280.1:p.Val99Leu
ENST00000468836.2:c.443G>C	ENSP00000419892.2:p.Arg148Pro
ENST00000644099.1:c.287G>C	ENSP00000494762.1:n.287G>C
ENST00000295911.6:c.67G>C	ENSP00000295911.2:p.Val23Leu
ENST00000327047.5:c.295G>C	ENSP00000322280.1:p.Val99Leu
ENST00000328863.8:c.295G>C	ENSP00000329158.4:p.Val99Leu
ENST00000468836.1:c.67G>C	ENSP00000419892.1:p.Val23Leu
ENST00000472224.1:n.301G>C
ENST00000485607.1:c.-42G>C	ENSP00000419244.1:n.-42G>C
ENST00000565169.1:c.24G>C
ENST00000569170.5:c.24G>C
NM_001195794.1:c.295G>C , LRG_700t1:c.295G>C	NP_001182723.1:p.Val99Leu
NM_001256819.1:c.467G>C	NP_001243748.1:p.Arg156Pro
NM_052995.2:c.67G>C , LRG_700t2:c.67G>C	NP_443721.1:p.Val23Leu
NM_174878.2:c.295G>C	NP_777367.1:p.Val99Leu
NR_046380.2:n.737G>C
XR_924167.1:n.607G>C
NM_001256819.2:c.467G>C	NP_001243748.1:p.Arg156Pro
NM_174878.3:c.295G>C MANE Select	NP_777367.1:p.Val99Leu
NR_046380.3:n.465G>C