Linked Data
COSMIC:
COSM5064229
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.106033558T>C , CM000685.2:g.106033558T>C | GRCh38 |
| NC_000023.10:g.105277549T>C , CM000685.1:g.105277549T>C | GRCh37 |
| NC_000023.9:g.105164205T>C | NCBI36 |
| NG_021252.1:g.10170A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000372563.2:c.1190A>G MANE Select | ENSP00000361644.1:p.Glu397Gly | |
| ENST00000327674.8:c.1190A>G | ENSP00000329374.4:p.Glu397Gly | |
| ENST00000372563.1:c.1190A>G | ENSP00000361644.1:p.Glu397Gly | |
| NM_000354.5:c.1190A>G | NP_000345.2:p.Glu397Gly | |
| XM_006724683.1:c.1220A>G | XP_006724746.1:p.Glu407Gly | |
| XM_005262180.4:c.*135A>G | XP_005262237.1:n.*135A>G | |
| XM_006724683.2:c.1220A>G | XP_006724746.1:p.Glu407Gly | |
| NM_000354.6:c.1190A>G MANE Select | NP_000345.2:p.Glu397Gly |