Linked Data
gnomAD v4:
5-137628310-G-A
COSMIC:
COSM735611
MyVariant Identifiers:
chr5:g.136963999G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.137628310G>A , CM000667.2:g.137628310G>A | GRCh38 |
| NC_000005.9:g.136963999G>A , CM000667.1:g.136963999G>A | GRCh37 |
| NC_000005.8:g.136991898G>A | NCBI36 |
| NG_032569.1:g.112781C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000309755.9:c.1578C>T MANE Select | ENSP00000312397.4:p.Cys526= | |
| ENST00000309755.8:c.1578C>T | ENSP00000312397.4:p.Cys526= | |
| ENST00000447439.6:n.1634C>T | ||
| ENST00000504208.5:c.*462C>T | ENSP00000423585.1:n.*462C>T | |
| ENST00000506491.5:c.1332C>T | ENSP00000424828.1:p.Cys444= | |
| ENST00000506873.5:n.1101C>T | ||
| ENST00000508657.5:c.1482C>T | ENSP00000422099.1:p.Cys494= | |
| ENST00000509694.1:n.371C>T | ||
| NM_001257194.1:c.1482C>T | NP_001244123.1:p.Cys494= | |
| NM_001257195.1:c.1332C>T | NP_001244124.1:p.Cys444= | |
| NM_017415.2:c.1578C>T | NP_059111.2:p.Cys526= | |
| NM_017415.3:c.1578C>T MANE Select | NP_059111.2:p.Cys526= | |
| NM_001257195.2:c.1332C>T | NP_001244124.1:p.Cys444= |