HGVS | Genome Assembly |
---|---|
NC_000002.12:g.47377029_47377032delinsGATC , CM000664.2:g.47377029_47377032delinsGATC | GRCh38 |
NC_000002.11:g.47604168_47604171delinsGATC , CM000664.1:g.47604168_47604171delinsGATC | GRCh37 |
NC_000002.10:g.47457672_47457675delinsGATC | NCBI36 |
NG_012352.2:g.36867_36870delinsGATC , LRG_215:g.36867_36870delinsGATC |
HGVS | Amino-acid change | |
---|---|---|
ENST00000263735.9:c.507_510delinsGATC MANE Select | ENSP00000263735.4:p.Glu169= | |
ENST00000263735.8:c.507_510delinsGATC | ENSP00000263735.4:p.Glu169= | |
ENST00000405271.5:c.591_594delinsGATC | ENSP00000385476.1:p.Glu197= | |
ENST00000456133.5:c.591_594delinsGATC | ENSP00000410675.1:p.Glu197= | |
ENST00000490733.1:n.356_359delinsGATC | ||
NM_002354.2:c.507_510delinsGATC , LRG_215t1:c.507_510delinsGATC | NP_002345.2:p.Glu169= | |
NM_002354.3:c.507_510delinsGATC MANE Select | NP_002345.2:p.Glu169= |