Linked Data
ClinVar Variation Id:
1661652
ClinVar RCV Id:
RCV002193185
dbSNP Id:
rs749457168
ExAC:
13:77574858 G / T
gnomAD v2:
13-77574858-G-T
gnomAD v3:
13-77000723-G-T
gnomAD v4:
13-77000723-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.77000723G>T , CM000675.2:g.77000723G>T | GRCh38 |
| NC_000013.10:g.77574858G>T , CM000675.1:g.77574858G>T | GRCh37 |
| NC_000013.9:g.76472859G>T | NCBI36 |
| NG_009064.1:g.13800G>T , LRG_692:g.13800G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000377453.9:c.831G>T (CLN5) MANE Select | ENSP00000366673.5:p.Gly277= | |
| ENST00000616833.6:c.*273G>T (CLN5) | ENSP00000479547.3:n.*273G>T | |
| ENST00000635838.1:c.174+4596G>T | ||
| ENST00000635905.1:n.566+4596G>T (CLN5) | ||
| ENST00000635915.1:c.829G>T (CLN5) | ||
| ENST00000636183.2:c.831G>T (CLN5) | ENSP00000490181.2:p.Gly277= | |
| ENST00000636525.2:c.565+4596G>T (CLN5) | ENSP00000490078.2:n.565+4596G>T | |
| ENST00000636681.1:c.*522G>T (CLN5) | ENSP00000489922.1:n.*522G>T | |
| ENST00000636705.1:c.667G>T (CLN5) | ||
| ENST00000636767.2:c.565+4596G>T (CLN5) | ENSP00000489855.2:n.565+4596G>T | |
| ENST00000636780.2:c.*280G>T (CLN5) | ENSP00000489809.2:n.*280G>T | |
| ENST00000637192.1:c.213+4596G>T | ||
| ENST00000637278.1:n.1157G>T (CLN5) | ||
| ENST00000637397.2:c.565+4596G>T (CLN5) | ENSP00000490422.2:n.565+4596G>T | |
| ENST00000638101.1:c.169+4596G>T | ENSP00000490535.1:n.169+4596G>T | |
| ENST00000638147.2:c.565+4596G>T | ENSP00000490953.2:n.565+4596G>T | |
| ENST00000377453.7:c.978G>T (CLN5) | ENSP00000366673.3:p.Gly326= | |
| ENST00000477982.2:n.1586C>A (FBXL3) | ||
| ENST00000485797.2:n.174-7772C>A (FBXL3) | ||
| ENST00000616833.4:c.831G>T (CLN5) | ENSP00000479547.1:p.Gly277= | |
| NM_006493.2:c.978G>T , LRG_692t1:c.978G>T (CLN5) | NP_006484.1:p.Gly326= | |
| XM_011534917.1:c.*280G>T (CLN5) | XP_011533219.1:n.*280G>T | |
| NM_001366624.1:c.*280G>T (CLN5) | NP_001353553.1:n.*280G>T | |
| NM_006493.3:c.831G>T (CLN5) | NP_006484.2:p.Gly277= | |
| XM_017020538.2:c.644-7772C>A (FBXL3) | XP_016876027.1:n.644-7772C>A | |
| NM_001366624.2:c.*280G>T (CLN5) | NP_001353553.1:n.*280G>T | |
| NM_006493.4:c.831G>T (CLN5) MANE Select | NP_006484.2:p.Gly277= |