Canonical Allele Identifier: CA355011924

Gene: CLRN1

Linked Data

• MyVariant Identifiers: chr3:g.150690330T>G (hg19) ; chr3:g.150972543T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.150972543T>G , CM000665.2:g.150972543T>G	GRCh38
NC_000003.11:g.150690330T>G , CM000665.1:g.150690330T>G	GRCh37
NC_000003.10:g.152173020T>G	NCBI36
NG_009168.1:g.5457A>C , LRG_700:g.5457A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327047.6:c.166A>C MANE Select	ENSP00000322280.1:p.Lys56Gln
ENST00000468836.2:c.142A>C	ENSP00000419892.2:p.Lys48Gln
ENST00000644099.1:c.7A>C	ENSP00000494762.1:p.Lys3Gln
ENST00000645441.1:c.8A>C
ENST00000327047.5:c.166A>C	ENSP00000322280.1:p.Lys56Gln
ENST00000328863.8:c.166A>C	ENSP00000329158.4:p.Lys56Gln
ENST00000468836.1:c.-235A>C	ENSP00000419892.1:n.-235A>C
ENST00000472224.1:n.172A>C
NM_001195794.1:c.166A>C , LRG_700t1:c.166A>C	NP_001182723.1:p.Lys56Gln
NM_001256819.1:c.166A>C	NP_001243748.1:p.Lys56Gln
NM_174878.2:c.166A>C	NP_777367.1:p.Lys56Gln
NR_046380.2:n.457A>C
XR_924167.1:n.478A>C
NM_001256819.2:c.166A>C	NP_001243748.1:p.Lys56Gln
NM_174878.3:c.166A>C MANE Select	NP_777367.1:p.Lys56Gln
NR_046380.3:n.185A>C