HGVS | Genome Assembly |
---|---|
NC_000012.12:g.110910995_110910998delinsCAGA , CM000674.2:g.110910995_110910998delinsCAGA | GRCh38 |
NC_000012.11:g.111348799_111348802delinsCAGA , CM000674.1:g.111348799_111348802delinsCAGA | GRCh37 |
NC_000012.10:g.109833182_109833185delinsCAGA | NCBI36 |
NG_007554.1:g.14580_14583delinsTCTG , LRG_393:g.14580_14583delinsTCTG |
HGVS | Amino-acid change | |
---|---|---|
ENST00000228841.15:c.*79_*82delinsTCTG MANE Select | ENSP00000228841.8:n.*79_*82delinsTCTG | |
ENST00000663220.1:c.*79_*82delinsTCTG | ENSP00000499568.1:n.*79_*82delinsTCTG | |
ENST00000228841.12:c.*79_*82delinsTCTG | ENSP00000228841.7:n.*79_*82delinsTCTG | |
ENST00000548438.1:c.*79_*82delinsTCTG | ENSP00000447154.1:n.*79_*82delinsTCTG | |
NM_000432.3:c.*79_*82delinsTCTG , LRG_393t1:c.*79_*82delinsTCTG | NP_000423.2:n.*79_*82delinsTCTG | |
NM_000432.4:c.*79_*82delinsTCTG MANE Select | NP_000423.2:n.*79_*82delinsTCTG |