Linked Data
COSMIC:
COSM1688554
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.152304554_152304555delinsAT , CM000663.2:g.152304554_152304555delinsAT | GRCh38 |
| NC_000001.10:g.152277030_152277031delinsAT , CM000663.1:g.152277030_152277031delinsAT | GRCh37 |
| NC_000001.9:g.150543654_150543655delinsAT | NCBI36 |
| NG_016190.1:g.25649_25650delinsAT , LRG_1028:g.25649_25650delinsAT |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000368799.2:c.10331_10332delinsAT MANE Select | ENSP00000357789.1:p.Gly3444Asp | |
| ENST00000368799.1:c.10331_10332delinsAT | ENSP00000357789.1:p.Gly3444Asp | |
| NM_002016.1:c.10331_10332delinsAT , LRG_1028t1:c.10331_10332delinsAT | NP_002007.1:p.Gly3444Asp | |
| XM_011509329.1:c.9109-722_9109-721delinsAT | XP_011507631.1:n.9109-722_9109-721delinsAT | |
| NM_002016.2:c.10331_10332delinsAT MANE Select | NP_002007.1:p.Gly3444Asp |