HGVS | Genome Assembly |
---|---|
NC_000001.11:g.94041338_94041339delinsC , CM000663.2:g.94041338_94041339delinsC | GRCh38 |
NC_000001.10:g.94506894_94506895delinsC , CM000663.1:g.94506894_94506895delinsC | GRCh37 |
NC_000001.9:g.94279482_94279483delinsC | NCBI36 |
NG_009073.1:g.84811_84812delinsG |
HGVS | Amino-acid change | |
---|---|---|
ENST00000370225.4:c.3392_3393delinsG MANE Select | ENSP00000359245.3:p.Ala1131GlyfsTer17 | |
ENST00000370225.3:c.3392_3393delinsG | ENSP00000359245.3:p.Ala1131GlyfsTer17 | |
ENST00000536513.5:c.-64-1250_-64-1249delinsG | ENSP00000439707.2:n.-64-1250_-64-1249deli... | |
NM_000350.2:c.3392_3393delinsG | NP_000341.2:p.Ala1131GlyfsTer17 | |
NM_000350.3:c.3392_3393delinsG MANE Select | NP_000341.2:p.Ala1131GlyfsTer17 |