HGVS | Genome Assembly |
---|---|
NC_000008.11:g.19958035_19958036insATTTA , CM000670.2:g.19958035_19958036insATTTA | GRCh38 |
NC_000008.10:g.19815546_19815547insATTTA , CM000670.1:g.19815546_19815547insATTTA | GRCh37 |
NC_000008.9:g.19859826_19859827insATTTA | NCBI36 |
NG_008855.1:g.23965_23966insATTTA | |
NG_008855.2:g.61319_61320insATTTA |
HGVS | Amino-acid change | |
---|---|---|
ENST00000650287.1:c.1019-1225_1019-1224insATTTA MANE Select | ENSP00000497642.1:n.1019-1225_1019-1224insATTTA | |
ENST00000650478.1:c.79+1952_79+1953insATTTA | ENSP00000497560.1:n.79+1952_79+1953insATTTA | |
ENST00000311322.8:c.1019-1225_1019-1224insATTTA | ENSP00000309757.6:n.1019-1225_1019-1224insATTTA | |
NM_000237.2:c.1019-1225_1019-1224insATTTA | NP_000228.1:n.1019-1225_1019-1224insATTTA | |
NM_000237.3:c.1019-1225_1019-1224insATTTA MANE Select | NP_000228.1:n.1019-1225_1019-1224insATTTA |