HGVS | Genome Assembly |
---|---|
NC_000001.11:g.204190617_204190618insTGCTG , CM000663.2:g.204190617_204190618insTGCTG | GRCh38 |
NC_000001.10:g.204159745_204159746insTGCTG , CM000663.1:g.204159745_204159746insTGCTG | GRCh37 |
NC_000001.9:g.202426368_202426369insTGCTG | NCBI36 |
NG_032151.1:g.10875_10876insAGCAC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000367194.5:c.284_285insAGCAC MANE Select | ENSP00000356162.4:p.Gln98HisfsTer? | |
ENST00000367194.4:c.284_285insAGCAC | ENSP00000356162.4:p.Gln98HisfsTer? | |
ENST00000625357.1:c.284_285insAGCAC | ENSP00000485957.1:p.Gln98HisfsTer? | |
NM_002256.3:c.284_285insAGCAC | NP_002247.3:p.Gln98HisfsTer? | |
XM_011509525.1:c.284_285insAGCAC | XP_011507827.1:p.Gln98HisfsTer? | |
NM_002256.4:c.284_285insAGCAC MANE Select | NP_002247.3:p.Gln98HisfsTer? |