HGVS | Genome Assembly |
---|---|
NC_000023.11:g.25013553_25013554insGGCCGC , CM000685.2:g.25013553_25013554insGGCCGC | GRCh38 |
NC_000023.10:g.25031670_25031671insGGCCGC , CM000685.1:g.25031670_25031671insGGCCGC | GRCh37 |
NC_000023.9:g.24941591_24941592insGGCCGC | NCBI36 |
NG_008281.1:g.7397_7398insGGCCGC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000379044.5:c.443_444insGGCCGC MANE Select | ENSP00000368332.4:p.Ala148_Ala149insAlaAla | |
ENST00000379044.4:c.443_444insGGCCGC | ENSP00000368332.4:p.Ala148_Ala149insAlaAla | |
NM_139058.2:c.443_444insGGCCGC | NP_620689.1:p.Ala148_Ala149insAlaAla | |
NM_139058.3:c.443_444insGGCCGC MANE Select | NP_620689.1:p.Ala148_Ala149insAlaAla |