Linked Data
dbSNP Id:
rs938552152
MyVariant Identifiers:
chr15:g.101455251_101455252insG (hg19)
chr15:g.100915046_100915047insG (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.100915046_100915047insG , CM000677.2:g.100915046_100915047insG | GRCh38 |
| NC_000015.9:g.101455251_101455252insG , CM000677.1:g.101455251_101455252insG | GRCh37 |
| NC_000015.8:g.99272774_99272775insG | NCBI36 |
| NG_012254.1:g.40243_40244insG | |
| NG_052791.1:g.1030_1031insG |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000329841.10:c.*273_*274insG (ALDH1A3) MANE Select | ENSP00000332256.5:n.*273_*274insG | |
| ENST00000329841.9:c.*273_*274insG (ALDH1A3) | ENSP00000332256.5:n.*273_*274insG | |
| ENST00000346623.6:c.*273_*274insG (ALDH1A3) | ENSP00000343294.6:n.*273_*274insG | |
| NM_000693.3:c.*273_*274insG (ALDH1A3) | NP_000684.2:n.*273_*274insG | |
| NM_001293815.1:c.*273_*274insG (ALDH1A3) | NP_001280744.1:n.*273_*274insG | |
| NR_135827.1:n.480+3757_480+3758insC (ALDH1A3-AS1) | ||
| NR_135828.1:n.1414_1415insC (ALDH1A3-AS1) | ||
| NR_135831.1:n.2330_2331insC (ALDH1A3-AS1) | ||
| NM_000693.4:c.*273_*274insG (ALDH1A3) MANE Select | NP_000684.2:n.*273_*274insG | |
| NM_001293815.2:c.*273_*274insG (ALDH1A3) | NP_001280744.1:n.*273_*274insG |