HGVS | Genome Assembly |
---|---|
NC_000016.10:g.89919688_89919690delinsATC , CM000678.2:g.89919688_89919690delinsATC | GRCh38 |
NC_000016.9:g.89986096_89986098delinsATC , CM000678.1:g.89986096_89986098delinsATC | GRCh37 |
NC_000016.8:g.88513597_88513599delinsATC | NCBI36 |
NG_012026.1:g.6810_6812delinsATC | |
NG_027810.1:g.2680_2682delinsATC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000555147.2:c.430_432delinsATC MANE Select | ENSP00000451605.1:p.Ile144= | |
ENST00000639847.1:c.430_432delinsATC | ENSP00000492011.1:p.Ile144= | |
ENST00000555147.1:c.430_432delinsATC | ENSP00000451605.1:p.Ile144= | |
ENST00000555427.1:c.430_432delinsATC | ENSP00000451760.1:p.Ile144= | |
ENST00000556922.1:c.430_432delinsATC | ENSP00000451560.1:p.Ile144= | |
NM_002386.3:c.430_432delinsATC | NP_002377.4:p.Ile144= | |
NM_002386.4:c.430_432delinsATC MANE Select | NP_002377.4:p.Ile144= |