Canonical Allele Identifier: CA275475

Linked Data

ClinVar Variation Id: 202192
ClinVar RCV Id: RCV000989150
dbSNP Id: rs794729218

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.76995933del , CM000675.2:g.76995933del GRCh38
NC_000013.10:g.77570068del , CM000675.1:g.77570068del GRCh37
NC_000013.9:g.76468069del NCBI36
NG_009064.1:g.9010del , LRG_692:g.9010del

Transcript Alleles

HGVS Amino-acid change
ENST00000377453.9:c.371del (CLN5) MANE Select ENSP00000366673.5:p.Ser124IlefsTer3
ENST00000485938.4:c.371del (CLN5) ENSP00000482959.3:p.Ser124IlefsTer3
ENST00000616833.6:c.371del (CLN5) ENSP00000479547.3:p.Ser124IlefsTer3
ENST00000635905.1:n.372del (CLN5)
ENST00000635915.1:c.369del (CLN5)
ENST00000635989.1:n.438del (CLN5)
ENST00000636183.2:c.371del (CLN5) ENSP00000490181.2:p.Ser124IlefsTer3
ENST00000636520.1:n.1883del (CLN5)
ENST00000636525.2:c.371del (CLN5) ENSP00000490078.2:p.Ser124IlefsTer3
ENST00000636602.1:n.317del (CLN5)
ENST00000636681.1:c.*62del (CLN5) ENSP00000489922.1:n.*62del
ENST00000636705.1:c.207del (CLN5)
ENST00000636767.2:c.371del (CLN5) ENSP00000489855.2:p.Ser124IlefsTer3
ENST00000636780.2:c.371del (CLN5) ENSP00000489809.2:p.Ser124IlefsTer3
ENST00000637192.1:c.19del
ENST00000637278.1:n.697del (CLN5)
ENST00000637397.2:c.371del (CLN5) ENSP00000490422.2:p.Ser124IlefsTer3
ENST00000637537.2:c.371del (CLN5) ENSP00000489711.2:p.Ser124IlefsTer3
ENST00000638147.2:c.371del ENSP00000490953.2:p.Ser124IlefsTer3
ENST00000377453.7:c.518del (CLN5) ENSP00000366673.3:p.Ser173IlefsTer3
ENST00000485797.2:n.174-2982del (FBXL3)
ENST00000485938.2:c.354del (CLN5)
ENST00000616833.4:c.371del (CLN5) ENSP00000479547.1:p.Ser124IlefsTer3
NM_006493.2:c.518del , LRG_692t1:c.518del (CLN5) NP_006484.1:p.Ser173IlefsTer3
XM_011534917.1:c.518del (CLN5) XP_011533219.1:p.Ser173IlefsTer3
NM_001366624.1:c.371del (CLN5) NP_001353553.1:p.Ser124IlefsTer3
NM_006493.3:c.371del (CLN5) NP_006484.2:p.Ser124IlefsTer3
XM_017020538.2:c.644-2982del (FBXL3) XP_016876027.1:n.644-2982del
NM_001366624.2:c.371del (CLN5) NP_001353553.1:p.Ser124IlefsTer3
NM_006493.4:c.371del (CLN5) MANE Select NP_006484.2:p.Ser124IlefsTer3