Canonical Allele Identifier: CA388308866

Linked Data

dbSNP Id: rs2034258749

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.76995967G>T , CM000675.2:g.76995967G>T GRCh38
NC_000013.10:g.77570102G>T , CM000675.1:g.77570102G>T GRCh37
NC_000013.9:g.76468103G>T NCBI36
NG_009064.1:g.9044G>T , LRG_692:g.9044G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000377453.9:c.405G>T (CLN5) MANE Select ENSP00000366673.5:p.Trp135Cys
ENST00000485938.4:c.405G>T (CLN5) ENSP00000482959.3:p.Trp135Cys
ENST00000616833.6:c.405G>T (CLN5) ENSP00000479547.3:p.Trp135Cys
ENST00000635838.1:c.14G>T
ENST00000635905.1:n.406G>T (CLN5)
ENST00000635915.1:c.403G>T (CLN5)
ENST00000635989.1:n.472G>T (CLN5)
ENST00000636183.2:c.405G>T (CLN5) ENSP00000490181.2:p.Trp135Cys
ENST00000636520.1:n.1917G>T (CLN5)
ENST00000636525.2:c.405G>T (CLN5) ENSP00000490078.2:p.Trp135Cys
ENST00000636602.1:n.351G>T (CLN5)
ENST00000636681.1:c.*96G>T (CLN5) ENSP00000489922.1:n.*96G>T
ENST00000636705.1:c.241G>T (CLN5)
ENST00000636767.2:c.405G>T (CLN5) ENSP00000489855.2:p.Trp135Cys
ENST00000636780.2:c.405G>T (CLN5) ENSP00000489809.2:p.Trp135Cys
ENST00000637192.1:c.53G>T
ENST00000637278.1:n.731G>T (CLN5)
ENST00000637397.2:c.405G>T (CLN5) ENSP00000490422.2:p.Trp135Cys
ENST00000637537.2:c.405G>T (CLN5) ENSP00000489711.2:p.Trp135Cys
ENST00000638101.1:c.9G>T ENSP00000490535.1:p.Trp3Cys
ENST00000638147.2:c.405G>T ENSP00000490953.2:p.Trp135Cys
ENST00000377453.7:c.552G>T (CLN5) ENSP00000366673.3:p.Trp184Cys
ENST00000485797.2:n.174-3016C>A (FBXL3)
ENST00000485938.2:c.388G>T (CLN5)
ENST00000616833.4:c.405G>T (CLN5) ENSP00000479547.1:p.Trp135Cys
NM_006493.2:c.552G>T , LRG_692t1:c.552G>T (CLN5) NP_006484.1:p.Trp184Cys
XM_011534917.1:c.552G>T (CLN5) XP_011533219.1:p.Trp184Cys
NM_001366624.1:c.405G>T (CLN5) NP_001353553.1:p.Trp135Cys
NM_006493.3:c.405G>T (CLN5) NP_006484.2:p.Trp135Cys
XM_017020538.2:c.644-3016C>A (FBXL3) XP_016876027.1:n.644-3016C>A
NM_001366624.2:c.405G>T (CLN5) NP_001353553.1:p.Trp135Cys
NM_006493.4:c.405G>T (CLN5) MANE Select NP_006484.2:p.Trp135Cys