Canonical Allele Identifier: CA2623303048

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.77000212_77000216del , CM000675.2:g.77000212_77000216del GRCh38
NC_000013.10:g.77574347_77574351del , CM000675.1:g.77574347_77574351del GRCh37
NC_000013.9:g.76472348_76472352del NCBI36
NG_009064.1:g.13289_13293del , LRG_692:g.13289_13293del

Transcript Alleles

HGVS Amino-acid Change
ENST00000377453.9:c.566-246_566-242del (CLN5) MANE Select ENSP00000366673.5:n.566-246_566-242del
ENST00000616833.6:c.*7+217_*7+221del (CLN5) ENSP00000479547.3:n.*7+217_*7+221del
ENST00000635761.1:n.378_382del (CLN5)
ENST00000635838.1:c.174+4085_174+4089del
ENST00000635905.1:n.566+4085_566+4089del (CLN5)
ENST00000635915.1:c.564-246_564-242del (CLN5)
ENST00000636183.2:c.566-246_566-242del (CLN5) ENSP00000490181.2:n.566-246_566-242del
ENST00000636525.2:c.565+4085_565+4089del (CLN5) ENSP00000490078.2:n.565+4085_565+4089del
ENST00000636681.1:c.*257-246_*257-242del (CLN5) ENSP00000489922.1:n.*257-246_*257-242del
ENST00000636705.1:c.402-246_402-242del (CLN5)
ENST00000636767.2:c.565+4085_565+4089del (CLN5) ENSP00000489855.2:n.565+4085_565+4089del
ENST00000636780.2:c.*15-246_*15-242del (CLN5) ENSP00000489809.2:n.*15-246_*15-242del
ENST00000637192.1:c.213+4085_213+4089del
ENST00000637278.1:n.892-246_892-242del (CLN5)
ENST00000637397.2:c.565+4085_565+4089del (CLN5) ENSP00000490422.2:n.565+4085_565+4089del
ENST00000638101.1:c.169+4085_169+4089del ENSP00000490535.1:n.169+4085_169+4089del
ENST00000638147.2:c.565+4085_565+4089del ENSP00000490953.2:n.565+4085_565+4089del
ENST00000377453.7:c.713-246_713-242del (CLN5) ENSP00000366673.3:n.713-246_713-242del
ENST00000477982.2:n.2096_2100del (FBXL3)
ENST00000485797.2:n.174-7262_174-7258del (FBXL3)
ENST00000616833.4:c.566-246_566-242del (CLN5) ENSP00000479547.1:n.566-246_566-242del
NM_006493.2:c.713-246_713-242del , LRG_692t1:c.713-246_713-242del (CLN5) NP_006484.1:n.713-246_713-242del
XM_011534917.1:c.*15-246_*15-242del (CLN5) XP_011533219.1:n.*15-246_*15-242del
NM_001366624.1:c.*15-246_*15-242del (CLN5) NP_001353553.1:n.*15-246_*15-242del
NM_006493.3:c.566-246_566-242del (CLN5) NP_006484.2:n.566-246_566-242del
XM_017020538.2:c.644-7262_644-7258del (FBXL3) XP_016876027.1:n.644-7262_644-7258del
NM_001366624.2:c.*15-246_*15-242del (CLN5) NP_001353553.1:n.*15-246_*15-242del
NM_006493.4:c.566-246_566-242del (CLN5) MANE Select NP_006484.2:n.566-246_566-242del