Canonical Allele Identifier: CA2103428750

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.76996258C= , CM000675.2:g.76996258C= GRCh38
NC_000013.10:g.77570393C= , CM000675.1:g.77570393C= GRCh37
NC_000013.9:g.76468394C= NCBI36
NG_009064.1:g.9335C= , LRG_692:g.9335C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000377453.9:c.565+131C= (CLN5) MANE Select ENSP00000366673.5:n.565+131C=
ENST00000485938.4:c.*120C= (CLN5) ENSP00000482959.3:n.*120C=
ENST00000616833.6:c.565+131C= (CLN5) ENSP00000479547.3:n.565+131C=
ENST00000635838.1:c.174+131C=
ENST00000635905.1:n.566+131C= (CLN5)
ENST00000635915.1:c.563+131C= (CLN5)
ENST00000636183.2:c.565+131C= (CLN5) ENSP00000490181.2:n.565+131C=
ENST00000636520.1:n.2208C= (CLN5)
ENST00000636525.2:c.565+131C= (CLN5) ENSP00000490078.2:n.565+131C=
ENST00000636602.1:n.642C= (CLN5)
ENST00000636681.1:c.*256+131C= (CLN5) ENSP00000489922.1:n.*256+131C=
ENST00000636705.1:c.401+131C= (CLN5)
ENST00000636767.2:c.565+131C= (CLN5) ENSP00000489855.2:n.565+131C=
ENST00000636780.2:c.565+131C= (CLN5) ENSP00000489809.2:n.565+131C=
ENST00000637192.1:c.213+131C=
ENST00000637278.1:n.891+131C= (CLN5)
ENST00000637397.2:c.565+131C= (CLN5) ENSP00000490422.2:n.565+131C=
ENST00000637537.2:c.565+131C= (CLN5) ENSP00000489711.2:n.565+131C=
ENST00000638101.1:c.169+131C= ENSP00000490535.1:n.169+131C=
ENST00000638147.2:c.565+131C= ENSP00000490953.2:n.565+131C=
ENST00000377453.7:c.712+131C= (CLN5) ENSP00000366673.3:n.712+131C=
ENST00000485797.2:n.174-3307G= (FBXL3)
ENST00000485938.2:c.679C= (CLN5)
ENST00000616833.4:c.565+131C= (CLN5) ENSP00000479547.1:n.565+131C=
NM_006493.2:c.712+131C= , LRG_692t1:c.712+131C= (CLN5) NP_006484.1:n.712+131C=
XM_011534917.1:c.712+131C= (CLN5) XP_011533219.1:n.712+131C=
NM_001366624.1:c.565+131C= (CLN5) NP_001353553.1:n.565+131C=
NM_006493.3:c.565+131C= (CLN5) NP_006484.2:n.565+131C=
XM_017020538.2:c.644-3307G= (FBXL3) XP_016876027.1:n.644-3307G=
NM_001366624.2:c.565+131C= (CLN5) NP_001353553.1:n.565+131C=
NM_006493.4:c.565+131C= (CLN5) MANE Select NP_006484.2:n.565+131C=