Canonical Allele Identifier: CA645583991

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.76996063dup , CM000675.2:g.76996063dup GRCh38
NC_000013.10:g.77570198dup , CM000675.1:g.77570198dup GRCh37
NC_000013.9:g.76468199dup NCBI36
NG_009064.1:g.9140dup , LRG_692:g.9140dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000377453.9:c.501dup (CLN5) MANE Select ENSP00000366673.5:p.Glu168Ter
ENST00000485938.4:c.501dup (CLN5) ENSP00000482959.3:p.Glu168Ter
ENST00000616833.6:c.501dup (CLN5) ENSP00000479547.3:p.Glu168Ter
ENST00000635838.1:c.110dup
ENST00000635905.1:n.502dup (CLN5)
ENST00000635915.1:c.499dup (CLN5)
ENST00000635989.1:n.568dup (CLN5)
ENST00000636183.2:c.501dup (CLN5) ENSP00000490181.2:p.Glu168Ter
ENST00000636520.1:n.2013dup (CLN5)
ENST00000636525.2:c.501dup (CLN5) ENSP00000490078.2:p.Glu168Ter
ENST00000636602.1:n.447dup (CLN5)
ENST00000636681.1:c.*192dup (CLN5) ENSP00000489922.1:n.*192dup
ENST00000636705.1:c.337dup (CLN5)
ENST00000636767.2:c.501dup (CLN5) ENSP00000489855.2:p.Glu168Ter
ENST00000636780.2:c.501dup (CLN5) ENSP00000489809.2:p.Glu168Ter
ENST00000637192.1:c.149dup
ENST00000637278.1:n.827dup (CLN5)
ENST00000637397.2:c.501dup (CLN5) ENSP00000490422.2:p.Glu168Ter
ENST00000637537.2:c.501dup (CLN5) ENSP00000489711.2:p.Glu168Ter
ENST00000638101.1:c.105dup ENSP00000490535.1:p.Glu36Ter
ENST00000638147.2:c.501dup ENSP00000490953.2:p.Glu168Ter
ENST00000377453.7:c.648dup (CLN5) ENSP00000366673.3:p.Glu217Ter
ENST00000485797.2:n.174-3107dup (FBXL3)
ENST00000485938.2:c.484dup (CLN5)
ENST00000616833.4:c.501dup (CLN5) ENSP00000479547.1:p.Glu168Ter
NM_006493.2:c.648dup , LRG_692t1:c.648dup (CLN5) NP_006484.1:p.Glu217Ter
XM_011534917.1:c.648dup (CLN5) XP_011533219.1:p.Glu217Ter
NM_001366624.1:c.501dup (CLN5) NP_001353553.1:p.Glu168Ter
NM_006493.3:c.501dup (CLN5) NP_006484.2:p.Glu168Ter
XM_017020538.2:c.644-3107dup (FBXL3) XP_016876027.1:n.644-3107dup
NM_001366624.2:c.501dup (CLN5) NP_001353553.1:p.Glu168Ter
NM_006493.4:c.501dup (CLN5) MANE Select NP_006484.2:p.Glu168Ter