HGVS | Genome Assembly |
---|---|
NC_000012.12:g.5044392_5044393insGGACCCGGGAGTGCGGCCCTTGCCTCCGCTGCCGGACTCGGGAGTGCGGCCCTTGCCTCCGCTGCCGGACCCGGGAGTGCGGCCCTTGCCTCCGCTGCC , CM000674.2:g.5044392_5044393insGGACCCGGGAGTGCGGCCCTTGCCTCCGCTGCCGGACTCGGGAGTGCGGCCCTTGCCTCCGCTGCCGGACCCGGGAGTGCGGCCCTTGCCTCCGCTGCC | GRCh38 |
NC_000012.11:g.5153558_5153559insGGACCCGGGAGTGCGGCCCTTGCCTCCGCTGCCGGACTCGGGAGTGCGGCCCTTGCCTCCGCTGCCGGACCCGGGAGTGCGGCCCTTGCCTCCGCTGCC , CM000674.1:g.5153558_5153559insGGACCCGGGAGTGCGGCCCTTGCCTCCGCTGCCGGACTCGGGAGTGCGGCCCTTGCCTCCGCTGCCGGACCCGGGAGTGCGGCCCTTGCCTCCGCTGCC | GRCh37 |
NC_000012.10:g.5023819_5023820insGGACCCGGGAGTGCGGCCCTTGCCTCCGCTGCCGGACTCGGGAGTGCGGCCCTTGCCTCCGCTGCCGGACCCGGGAGTGCGGCCCTTGCCTCCGCTGCC | NCBI36 |
NG_012198.1:g.5474_5475insGGACCCGGGAGTGCGGCCCTTGCCTCCGCTGCCGGACTCGGGAGTGCGGCCCTTGCCTCCGCTGCCGGACCCGGGAGTGCGGCCCTTGCCTCCGCTGCC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000252321.5:c.245_246insGGACCCGGGAGTGCGGCCCTTGCCTCCGCTGCCGGACTCGGGAGTGCGGCCCTTGCCTCCGCTGCCGGACCCGGGAGTGCGGCCCTTGCCTCCGCTGCC MANE Select | ENSP00000252321.3:p.Pro82_Glu83insAspProGlyValArgProLeuProPro... | |
ENST00000252321.4:c.245_246insGGACCCGGGAGTGCGGCCCTTGCCTCCGCTGCCGGACTCGGGAGTGCGGCCCTTGCCTCCGCTGCCGGACCCGGGAGTGCGGCCCTTGCCTCCGCTGCC | ENSP00000252321.3:p.Pro82_Glu83insAspProGlyValArgProLeuProPro... | |
NM_002234.3:c.245_246insGGACCCGGGAGTGCGGCCCTTGCCTCCGCTGCCGGACTCGGGAGTGCGGCCCTTGCCTCCGCTGCCGGACCCGGGAGTGCGGCCCTTGCCTCCGCTGCC | NP_002225.2:p.Pro82_Glu83insAspProGlyValArgProLeuProProLeuPro... | |
NM_002234.4:c.245_246insGGACCCGGGAGTGCGGCCCTTGCCTCCGCTGCCGGACTCGGGAGTGCGGCCCTTGCCTCCGCTGCCGGACCCGGGAGTGCGGCCCTTGCCTCCGCTGCC MANE Select | NP_002225.2:p.Pro82_Glu83insAspProGlyValArgProLeuProProLeuPro... |