Canonical Allele Identifier: CA957798891

Linked Data

dbSNP Id: rs2034266783

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.76996261dup , CM000675.2:g.76996261dup GRCh38
NC_000013.10:g.77570396dup , CM000675.1:g.77570396dup GRCh37
NC_000013.9:g.76468397dup NCBI36
NG_009064.1:g.9338dup , LRG_692:g.9338dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000377453.9:c.565+134dup (CLN5) MANE Select ENSP00000366673.5:n.565+134dup
ENST00000485938.4:c.*123dup (CLN5) ENSP00000482959.3:n.*123dup
ENST00000616833.6:c.565+134dup (CLN5) ENSP00000479547.3:n.565+134dup
ENST00000635838.1:c.174+134dup
ENST00000635905.1:n.566+134dup (CLN5)
ENST00000635915.1:c.563+134dup (CLN5)
ENST00000636183.2:c.565+134dup (CLN5) ENSP00000490181.2:n.565+134dup
ENST00000636520.1:n.2211dup (CLN5)
ENST00000636525.2:c.565+134dup (CLN5) ENSP00000490078.2:n.565+134dup
ENST00000636602.1:n.645dup (CLN5)
ENST00000636681.1:c.*256+134dup (CLN5) ENSP00000489922.1:n.*256+134dup
ENST00000636705.1:c.401+134dup (CLN5)
ENST00000636767.2:c.565+134dup (CLN5) ENSP00000489855.2:n.565+134dup
ENST00000636780.2:c.565+134dup (CLN5) ENSP00000489809.2:n.565+134dup
ENST00000637192.1:c.213+134dup
ENST00000637278.1:n.891+134dup (CLN5)
ENST00000637397.2:c.565+134dup (CLN5) ENSP00000490422.2:n.565+134dup
ENST00000637537.2:c.565+134dup (CLN5) ENSP00000489711.2:n.565+134dup
ENST00000638101.1:c.169+134dup ENSP00000490535.1:n.169+134dup
ENST00000638147.2:c.565+134dup ENSP00000490953.2:n.565+134dup
ENST00000377453.7:c.712+134dup (CLN5) ENSP00000366673.3:n.712+134dup
ENST00000485797.2:n.174-3309dup (FBXL3)
ENST00000485938.2:c.682dup (CLN5)
ENST00000616833.4:c.565+134dup (CLN5) ENSP00000479547.1:n.565+134dup
NM_006493.2:c.712+134dup , LRG_692t1:c.712+134dup (CLN5) NP_006484.1:n.712+134dup
XM_011534917.1:c.712+134dup (CLN5) XP_011533219.1:n.712+134dup
NM_001366624.1:c.565+134dup (CLN5) NP_001353553.1:n.565+134dup
NM_006493.3:c.565+134dup (CLN5) NP_006484.2:n.565+134dup
XM_017020538.2:c.644-3309dup (FBXL3) XP_016876027.1:n.644-3309dup
NM_001366624.2:c.565+134dup (CLN5) NP_001353553.1:n.565+134dup
NM_006493.4:c.565+134dup (CLN5) MANE Select NP_006484.2:n.565+134dup