HGVS | Genome Assembly |
---|---|
NC_000006.12:g.49459052_49459053delinsTA , CM000668.2:g.49459052_49459053delinsTA | GRCh38 |
NC_000006.11:g.49426765_49426766delinsTA , CM000668.1:g.49426765_49426766delinsTA | GRCh37 |
NC_000006.10:g.49534724_49534725delinsTA | NCBI36 |
NG_007100.1:g.9087_9088delinsTA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000274813.4:c.385+29_385+30delinsTA MANE Select | ENSP00000274813.3:n.385+29_385+30delinsTA | |
ENST00000274813.3:c.385+29_385+30delinsTA | ENSP00000274813.3:n.385+29_385+30delinsTA | |
NM_000255.3:c.385+29_385+30delinsTA | NP_000246.2:n.385+29_385+30delinsTA | |
XM_005249143.2:c.385+29_385+30delinsTA | XP_005249200.1:n.385+29_385+30delinsTA | |
XM_005249143.3:c.385+29_385+30delinsTA | XP_005249200.1:n.385+29_385+30delinsTA | |
NM_000255.4:c.385+29_385+30delinsTA MANE Select | NP_000246.2:n.385+29_385+30delinsTA |