HGVS | Genome Assembly |
---|---|
NC_000016.10:g.89919922_89919923delinsTA , CM000678.2:g.89919922_89919923delinsTA | GRCh38 |
NC_000016.9:g.89986330_89986331delinsTA , CM000678.1:g.89986330_89986331delinsTA | GRCh37 |
NC_000016.8:g.88513831_88513832delinsTA | NCBI36 |
NG_012026.1:g.7044_7045delinsTA | |
NG_027810.1:g.2914_2915delinsTA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000555147.2:c.664_665delinsTA MANE Select | ENSP00000451605.1:p.Ala222Tyr | |
ENST00000639847.1:c.664_665delinsTA | ENSP00000492011.1:p.Ala222Tyr | |
ENST00000555147.1:c.664_665delinsTA | ENSP00000451605.1:p.Ala222Tyr | |
ENST00000555427.1:c.664_665delinsTA | ENSP00000451760.1:p.Ala222Tyr | |
ENST00000556922.1:c.664_665delinsTA | ENSP00000451560.1:p.Ala222Tyr | |
NM_002386.3:c.664_665delinsTA | NP_002377.4:p.Ala222Tyr | |
NM_002386.4:c.664_665delinsTA MANE Select | NP_002377.4:p.Ala222Tyr |