Canonical Allele Identifier: CA354955431
Gene: CLRN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.150941617C>G , CM000665.2:g.150941617C>G GRCh38
NC_000003.11:g.150659404C>G , CM000665.1:g.150659404C>G GRCh37
NC_000003.10:g.152142094C>G NCBI36
NG_009168.1:g.36383G>C , LRG_700:g.36383G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000327047.6:c.398G>C MANE Select ENSP00000322280.1:p.Gly133Ala
ENST00000468836.2:c.546G>C ENSP00000419892.2:n.546G>C
ENST00000644099.1:c.390G>C ENSP00000494762.1:n.390G>C
ENST00000295911.6:c.170G>C ENSP00000295911.2:p.Gly57Ala
ENST00000327047.5:c.398G>C ENSP00000322280.1:p.Gly133Ala
ENST00000328863.8:c.398G>C ENSP00000329158.4:p.Gly133Ala
ENST00000468836.1:c.170G>C ENSP00000419892.1:p.Gly57Ala
ENST00000472224.1:n.404G>C
ENST00000485607.1:c.62G>C ENSP00000419244.1:p.Gly21Ala
ENST00000562308.5:c.69G>C
ENST00000565169.1:c.127G>C
ENST00000569170.5:c.127G>C
NM_001195794.1:c.398G>C , LRG_700t1:c.398G>C NP_001182723.1:p.Gly133Ala
NM_001256819.1:c.*12G>C NP_001243748.1:n.*12G>C
NM_052995.2:c.170G>C , LRG_700t2:c.170G>C NP_443721.1:p.Gly57Ala
NM_174878.2:c.398G>C NP_777367.1:p.Gly133Ala
NR_046380.2:n.840G>C
XR_924167.1:n.710G>C
NM_001256819.2:c.*12G>C NP_001243748.1:n.*12G>C
NM_174878.3:c.398G>C MANE Select NP_777367.1:p.Gly133Ala
NR_046380.3:n.568G>C