Canonical Allele Identifier: CA354955270

Gene: CLRN1

Linked Data

• MyVariant Identifiers: chr3:g.150659371G>C (hg19) ; chr3:g.150941584G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.150941584G>C , CM000665.2:g.150941584G>C	GRCh38
NC_000003.11:g.150659371G>C , CM000665.1:g.150659371G>C	GRCh37
NC_000003.10:g.152142061G>C	NCBI36
NG_009168.1:g.36416C>G , LRG_700:g.36416C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327047.6:c.431C>G MANE Select	ENSP00000322280.1:p.Ser144Ter
ENST00000468836.2:c.579C>G	ENSP00000419892.2:n.579C>G
ENST00000644099.1:c.423C>G	ENSP00000494762.1:n.423C>G
ENST00000295911.6:c.203C>G	ENSP00000295911.2:p.Ser68Ter
ENST00000327047.5:c.431C>G	ENSP00000322280.1:p.Ser144Ter
ENST00000328863.8:c.431C>G	ENSP00000329158.4:p.Ser144Ter
ENST00000468836.1:c.203C>G	ENSP00000419892.1:p.Ser68Ter
ENST00000472224.1:n.437C>G
ENST00000485607.1:c.95C>G	ENSP00000419244.1:p.Ser32Ter
ENST00000562308.5:c.102C>G
ENST00000565169.1:c.160C>G
ENST00000569170.5:c.160C>G
NM_001195794.1:c.431C>G , LRG_700t1:c.431C>G	NP_001182723.1:p.Ser144Ter
NM_001256819.1:c.*45C>G	NP_001243748.1:n.*45C>G
NM_052995.2:c.203C>G , LRG_700t2:c.203C>G	NP_443721.1:p.Ser68Ter
NM_174878.2:c.431C>G	NP_777367.1:p.Ser144Ter
NR_046380.2:n.873C>G
XR_924167.1:n.743C>G
NM_001256819.2:c.*45C>G	NP_001243748.1:n.*45C>G
NM_174878.3:c.431C>G MANE Select	NP_777367.1:p.Ser144Ter
NR_046380.3:n.601C>G