HGVS | Genome Assembly |
---|---|
NC_000011.10:g.5227011_5227012delinsTT , CM000673.2:g.5227011_5227012delinsTT | GRCh38 |
NC_000011.9:g.5248241_5248242delinsTT , CM000673.1:g.5248241_5248242delinsTT | GRCh37 |
NC_000011.8:g.5204817_5204818delinsTT | NCBI36 |
NG_000007.3:g.70604_70605delinsAA | |
NG_059281.1:g.5060_5061delinsAA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000647020.1:c.10_11delinsAA | ENSP00000494175.1:p.Leu4Lys | |
ENST00000335295.4:c.10_11delinsAA MANE Select | ENSP00000333994.3:p.Leu4Lys | |
ENST00000380315.2:c.10_11delinsAA | ENSP00000369671.2:p.Leu4Lys | |
ENST00000485743.1:n.61_62delinsAA | ||
ENST00000633227.1:c.10_11delinsAA | ENSP00000488004.1:p.Leu4Lys | |
NM_000518.4:c.10_11delinsAA | NP_000509.1:p.Leu4Lys | |
NM_000518.5:c.10_11delinsAA MANE Select | NP_000509.1:p.Leu4Lys |