Canonical Allele Identifier: CA1054916398
Gene: CLRN1 HGNC NCBI

Linked Data

dbSNP Id: rs904951442

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.150941921G>A , CM000665.2:g.150941921G>A GRCh38
NC_000003.11:g.150659708G>A , CM000665.1:g.150659708G>A GRCh37
NC_000003.10:g.152142398G>A NCBI36
NG_009168.1:g.36079C>T , LRG_700:g.36079C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000327047.6:c.254-160C>T MANE Select ENSP00000322280.1:n.254-160C>T
ENST00000468836.2:c.402-160C>T ENSP00000419892.2:n.402-160C>T
ENST00000644099.1:c.246-160C>T ENSP00000494762.1:n.246-160C>T
ENST00000295911.6:c.26-160C>T ENSP00000295911.2:n.26-160C>T
ENST00000327047.5:c.254-160C>T ENSP00000322280.1:n.254-160C>T
ENST00000328863.8:c.254-160C>T ENSP00000329158.4:n.254-160C>T
ENST00000468836.1:c.26-160C>T ENSP00000419892.1:n.26-160C>T
ENST00000472224.1:n.260-160C>T
ENST00000485607.1:c.-83-160C>T ENSP00000419244.1:n.-83-160C>T
NM_001195794.1:c.254-160C>T , LRG_700t1:c.254-160C>T NP_001182723.1:n.254-160C>T
NM_001256819.1:c.426-160C>T NP_001243748.1:n.426-160C>T
NM_052995.2:c.26-160C>T , LRG_700t2:c.26-160C>T NP_443721.1:n.26-160C>T
NM_174878.2:c.254-160C>T NP_777367.1:n.254-160C>T
NR_046380.2:n.696-160C>T
XR_924167.1:n.566-160C>T
NM_001256819.2:c.426-160C>T NP_001243748.1:n.426-160C>T
NM_174878.3:c.254-160C>T MANE Select NP_777367.1:n.254-160C>T
NR_046380.3:n.424-160C>T