Canonical Allele Identifier: CA355011911

Gene: CLRN1

Linked Data

• MyVariant Identifiers: chr3:g.150690326A>C (hg19) ; chr3:g.150972539A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.150972539A>C , CM000665.2:g.150972539A>C	GRCh38
NC_000003.11:g.150690326A>C , CM000665.1:g.150690326A>C	GRCh37
NC_000003.10:g.152173016A>C	NCBI36
NG_009168.1:g.5461T>G , LRG_700:g.5461T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327047.6:c.170T>G MANE Select	ENSP00000322280.1:p.Phe57Cys
ENST00000468836.2:c.146T>G	ENSP00000419892.2:p.Phe49Cys
ENST00000644099.1:c.11T>G	ENSP00000494762.1:p.Phe4Cys
ENST00000645441.1:c.12T>G
ENST00000327047.5:c.170T>G	ENSP00000322280.1:p.Phe57Cys
ENST00000328863.8:c.170T>G	ENSP00000329158.4:p.Phe57Cys
ENST00000468836.1:c.-231T>G	ENSP00000419892.1:n.-231T>G
ENST00000472224.1:n.176T>G
NM_001195794.1:c.170T>G , LRG_700t1:c.170T>G	NP_001182723.1:p.Phe57Cys
NM_001256819.1:c.170T>G	NP_001243748.1:p.Phe57Cys
NM_174878.2:c.170T>G	NP_777367.1:p.Phe57Cys
NR_046380.2:n.461T>G
XR_924167.1:n.482T>G
NM_001256819.2:c.170T>G	NP_001243748.1:p.Phe57Cys
NM_174878.3:c.170T>G MANE Select	NP_777367.1:p.Phe57Cys
NR_046380.3:n.189T>G