Linked Data
dbSNP Id:
rs1253887837
MyVariant Identifiers:
chr15:g.38644455_38644456insTATG (hg19)
chr15:g.38352254_38352255insTATG (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.38352257_38352258insGTAT , CM000677.2:g.38352257_38352258insGTAT | GRCh38 |
| NC_000015.9:g.38644458_38644459insGTAT , CM000677.1:g.38644458_38644459insGTAT | GRCh37 |
| NC_000015.8:g.36431750_36431751insGTAT | NCBI36 |
| NG_008980.1:g.104407_104408insGTAT |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000299084.9:c.*593_*594insGTAT MANE Select | ENSP00000299084.4:n.*593_*594insGTAT | |
| ENST00000299084.8:c.*593_*594insGTAT | ENSP00000299084.4:n.*593_*594insGTAT | |
| NM_152594.2:c.*593_*594insGTAT | NP_689807.1:n.*593_*594insGTAT | |
| XM_005254202.2:c.*593_*594insGTAT | XP_005254259.1:n.*593_*594insGTAT | |
| XM_005254203.3:c.*593_*594insGTAT | XP_005254260.1:n.*593_*594insGTAT | |
| XM_011521288.1:c.*593_*594insGTAT | XP_011519590.1:n.*593_*594insGTAT | |
| XM_011521289.1:c.*593_*594insGTAT | XP_011519591.1:n.*593_*594insGTAT | |
| XM_011521290.1:c.*593_*594insGTAT | XP_011519592.1:n.*593_*594insGTAT | |
| XM_005254202.3:c.*593_*594insGTAT | XP_005254259.1:n.*593_*594insGTAT | |
| XM_011521289.3:c.*593_*594insGTAT | XP_011519591.1:n.*593_*594insGTAT | |
| NM_152594.3:c.*593_*594insGTAT MANE Select | NP_689807.1:n.*593_*594insGTAT |