Linked Data
dbSNP Id:
rs72512864
MyVariant Identifiers:
chr10:g.71218016_71218017insGAG (hg19)
chr10:g.69458260_69458261insGAG (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.69458262_69458263insGGA , CM000672.2:g.69458262_69458263insGGA | GRCh38 |
| NC_000010.10:g.71218018_71218019insGGA , CM000672.1:g.71218018_71218019insGGA | GRCh37 |
| NC_000010.9:g.70888024_70888025insGGA | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000373290.7:c.96+6572_96+6573insGGA MANE Select | ENSP00000362387.2:n.96+6572_96+6573insGGA | |
| ENST00000373290.6:c.96+6572_96+6573insGGA | ENSP00000362387.2:n.96+6572_96+6573insGGA | |
| ENST00000478112.1:n.214+6572_214+6573insGGA | ||
| NM_012339.3:c.96+6572_96+6573insGGA | NP_036471.1:n.96+6572_96+6573insGGA | |
| XM_005269667.3:c.96+6572_96+6573insGGA | XP_005269724.1:n.96+6572_96+6573insGGA | |
| XM_006717738.2:c.25-25429_25-25428insGGA | XP_006717801.1:n.25-25429_25-25428insGGA | |
| XR_945642.1:n.226+6572_226+6573insGGA | ||
| NM_001351263.1:c.96+6572_96+6573insGGA | NP_001338192.1:n.96+6572_96+6573insGGA | |
| NM_012339.4:c.96+6572_96+6573insGGA | NP_036471.1:n.96+6572_96+6573insGGA | |
| NR_147091.1:n.224+6572_224+6573insGGA | ||
| XM_017016010.1:c.96+6572_96+6573insGGA | XP_016871499.1:n.96+6572_96+6573insGGA | |
| XR_001747072.1:n.227+6572_227+6573insGGA | ||
| XR_001747073.1:n.227+6572_227+6573insGGA | ||
| XR_001747074.1:n.224+6572_224+6573insGGA | ||
| NM_012339.5:c.96+6572_96+6573insGGA MANE Select | NP_036471.1:n.96+6572_96+6573insGGA | |
| NM_001351263.2:c.96+6572_96+6573insGGA | NP_001338192.1:n.96+6572_96+6573insGGA | |
| NR_147091.2:n.226+6572_226+6573insGGA |