HGVS | Genome Assembly |
---|---|
NC_000008.11:g.38144287_38144288insG , CM000670.2:g.38144287_38144288insG | GRCh38 |
NC_000008.10:g.38001805_38001806insG , CM000670.1:g.38001805_38001806insG | GRCh37 |
NC_000008.9:g.38120962_38120963insG | NCBI36 |
NG_011827.1:g.11795_11796insC |
HGVS | Amino-acid change | |
---|---|---|
ENST00000276449.9:c.843_844insC MANE Select | ENSP00000276449.3:p.Glu282ArgfsTer? | |
ENST00000276449.8:c.843_844insC | ENSP00000276449.3:p.Glu282ArgfsTer? | |
ENST00000520114.1:n.2812_2813insC | ||
ENST00000522050.1:c.685_686insC | ||
NM_000349.2:c.843_844insC | NP_000340.2:p.Glu282ArgfsTer? | |
XM_006716392.1:c.749_750insC | XP_006716455.1:p.Lys251GlufsTer5 | |
NM_000349.3:c.843_844insC MANE Select | NP_000340.2:p.Glu282ArgfsTer? |