HGVS | Genome Assembly |
---|---|
NC_000016.10:g.173600_173601delinsAG , CM000678.2:g.173600_173601delinsAG | GRCh38 |
NC_000016.9:g.223599_223600delinsAG , CM000678.1:g.223599_223600delinsAG | GRCh37 |
NC_000016.8:g.163599_163600delinsAG | NCBI36 |
NG_000006.1:g.34463_34464delinsAG | |
NG_059186.1:g.1950_1951delinsAG | |
NG_059271.1:g.5754_5755delinsAG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000251595.11:c.429_*1delinsAG MANE Select | ENSP00000251595.6:n.[c.429_*1delinsAG;Ter143=] | |
ENST00000251595.10:c.429_*1delinsAG | ENSP00000251595.6:n.[c.429_*1delinsAG;Ter143=] | |
ENST00000397806.1:c.333_*1delinsAG | ENSP00000380908.1:n.[c.333_*1delinsAG;Ter111=] | |
ENST00000482565.1:n.565_566delinsAG | ||
NM_000517.4:c.429_*1delinsAG | NP_000508.1:n.[c.429_*1delinsAG;Ter143=] | |
NM_000517.6:c.429_*1delinsAG MANE Select | NP_000508.1:n.[c.429_*1delinsAG;Ter143=] |