Canonical Allele Identifier: CA354955598
Gene: CLRN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.150941663A>G , CM000665.2:g.150941663A>G GRCh38
NC_000003.11:g.150659450A>G , CM000665.1:g.150659450A>G GRCh37
NC_000003.10:g.152142140A>G NCBI36
NG_009168.1:g.36337T>C , LRG_700:g.36337T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000327047.6:c.352T>C MANE Select ENSP00000322280.1:p.Phe118Leu
ENST00000468836.2:c.500T>C ENSP00000419892.2:p.Leu167Pro
ENST00000644099.1:c.344T>C ENSP00000494762.1:n.344T>C
ENST00000295911.6:c.124T>C ENSP00000295911.2:p.Phe42Leu
ENST00000327047.5:c.352T>C ENSP00000322280.1:p.Phe118Leu
ENST00000328863.8:c.352T>C ENSP00000329158.4:p.Phe118Leu
ENST00000468836.1:c.124T>C ENSP00000419892.1:p.Phe42Leu
ENST00000472224.1:n.358T>C
ENST00000485607.1:c.16T>C ENSP00000419244.1:p.Phe6Leu
ENST00000562308.5:c.23T>C
ENST00000565169.1:c.81T>C
ENST00000569170.5:c.81T>C
NM_001195794.1:c.352T>C , LRG_700t1:c.352T>C NP_001182723.1:p.Phe118Leu
NM_001256819.1:c.524T>C NP_001243748.1:p.Leu175Pro
NM_052995.2:c.124T>C , LRG_700t2:c.124T>C NP_443721.1:p.Phe42Leu
NM_174878.2:c.352T>C NP_777367.1:p.Phe118Leu
NR_046380.2:n.794T>C
XR_924167.1:n.664T>C
NM_001256819.2:c.524T>C NP_001243748.1:p.Leu175Pro
NM_174878.3:c.352T>C MANE Select NP_777367.1:p.Phe118Leu
NR_046380.3:n.522T>C