HGVS | Genome Assembly |
---|---|
NC_000017.11:g.4898675_4898676insA , CM000679.2:g.4898675_4898676insA | GRCh38 |
NC_000017.10:g.4801970_4801971insA , CM000679.1:g.4801970_4801971insA | GRCh37 |
NC_000017.9:g.4742749_4742750insA | NCBI36 |
NG_008029.2:g.9400_9401insT | |
NG_028005.1:g.70336_70337insA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000649488.2:c.*60_*61insT MANE Select | ENSP00000497829.1:n.*60_*61insT | |
ENST00000649830.1:c.*178_*179insT | ENSP00000496907.1:n.*178_*179insT | |
ENST00000652550.1:n.1268_1269insT | ||
ENST00000293780.4:c.*60_*61insT | ENSP00000293780.4:n.*60_*61insT | |
ENST00000572438.1:n.1228_1229insT | ||
NM_000080.3:c.*60_*61insT | NP_000071.1:n.*60_*61insT | |
NM_000080.4:c.*60_*61insT MANE Select | NP_000071.1:n.*60_*61insT | |
XM_017024115.1:c.*60_*61insT | XP_016879604.1:n.*60_*61insT |