Canonical Allele Identifier: CA354955385
Gene: CLRN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.150941605A>T , CM000665.2:g.150941605A>T GRCh38
NC_000003.11:g.150659392A>T , CM000665.1:g.150659392A>T GRCh37
NC_000003.10:g.152142082A>T NCBI36
NG_009168.1:g.36395T>A , LRG_700:g.36395T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000327047.6:c.410T>A MANE Select ENSP00000322280.1:p.Leu137Gln
ENST00000468836.2:c.558T>A ENSP00000419892.2:n.558T>A
ENST00000644099.1:c.402T>A ENSP00000494762.1:n.402T>A
ENST00000295911.6:c.182T>A ENSP00000295911.2:p.Leu61Gln
ENST00000327047.5:c.410T>A ENSP00000322280.1:p.Leu137Gln
ENST00000328863.8:c.410T>A ENSP00000329158.4:p.Leu137Gln
ENST00000468836.1:c.182T>A ENSP00000419892.1:p.Leu61Gln
ENST00000472224.1:n.416T>A
ENST00000485607.1:c.74T>A ENSP00000419244.1:p.Leu25Gln
ENST00000562308.5:c.81T>A
ENST00000565169.1:c.139T>A
ENST00000569170.5:c.139T>A
NM_001195794.1:c.410T>A , LRG_700t1:c.410T>A NP_001182723.1:p.Leu137Gln
NM_001256819.1:c.*24T>A NP_001243748.1:n.*24T>A
NM_052995.2:c.182T>A , LRG_700t2:c.182T>A NP_443721.1:p.Leu61Gln
NM_174878.2:c.410T>A NP_777367.1:p.Leu137Gln
NR_046380.2:n.852T>A
XR_924167.1:n.722T>A
NM_001256819.2:c.*24T>A NP_001243748.1:n.*24T>A
NM_174878.3:c.410T>A MANE Select NP_777367.1:p.Leu137Gln
NR_046380.3:n.580T>A