Canonical Allele Identifier: CA2605478326
Gene: CLRN1 HGNC NCBI

Linked Data

dbSNP Id: rs79756115

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.150940779C>T , CM000665.2:g.150940779C>T GRCh38
NC_000003.11:g.150658566C>T , CM000665.1:g.150658566C>T GRCh37
NC_000003.10:g.152141256C>T NCBI36
NG_009168.1:g.37221G>A , LRG_700:g.37221G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000327047.6:c.433+803G>A MANE Select ENSP00000322280.1:n.433+803G>A
ENST00000468836.2:c.581+803G>A ENSP00000419892.2:n.581+803G>A
ENST00000644099.1:c.426-260G>A ENSP00000494762.1:n.426-260G>A
ENST00000295911.6:c.205+803G>A ENSP00000295911.2:n.205+803G>A
ENST00000327047.5:c.433+803G>A ENSP00000322280.1:n.433+803G>A
ENST00000328863.8:c.434-260G>A ENSP00000329158.4:n.434-260G>A
ENST00000468836.1:c.205+803G>A ENSP00000419892.1:n.205+803G>A
ENST00000485607.1:c.97+803G>A ENSP00000419244.1:n.97+803G>A
ENST00000562308.5:c.104+803G>A
ENST00000565169.1:c.162+803G>A
ENST00000569170.5:c.162+803G>A
NM_001195794.1:c.434-260G>A , LRG_700t1:c.434-260G>A NP_001182723.1:n.434-260G>A
NM_001256819.1:c.*47+803G>A NP_001243748.1:n.*47+803G>A
NM_052995.2:c.205+803G>A , LRG_700t2:c.205+803G>A NP_443721.1:n.205+803G>A
NM_174878.2:c.433+803G>A NP_777367.1:n.433+803G>A
NR_046380.2:n.876-260G>A
XR_924167.1:n.745+803G>A
NM_001256819.2:c.*47+803G>A NP_001243748.1:n.*47+803G>A
NM_174878.3:c.433+803G>A MANE Select NP_777367.1:n.433+803G>A
NR_046380.3:n.604-260G>A