HGVS | Genome Assembly |
---|---|
NC_000010.11:g.94782213_94782214delinsTA , CM000672.2:g.94782213_94782214delinsTA | GRCh38 |
NC_000010.10:g.96541970_96541971delinsTA , CM000672.1:g.96541970_96541971delinsTA | GRCh37 |
NC_000010.9:g.96531960_96531961delinsTA | NCBI36 |
NG_008384.2:g.24508_24509delinsTA | |
NG_008384.3:g.24533_24534delinsTA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000371321.9:c.819+216_819+217delinsTA MANE Select | ENSP00000360372.3:n.819+216_819+217delinsTA | |
ENST00000645461.1:n.1872+216_1872+217delinsTA | ||
ENST00000371321.7:c.819+216_819+217delinsTA | ENSP00000360372.3:n.819+216_819+217delinsTA | |
ENST00000464755.1:c.1582+216_1582+217delinsTA | ENSP00000483243.1:n.1582+216_1582+217delinsTA | |
NM_000769.2:c.819+216_819+217delinsTA | NP_000760.1:n.819+216_819+217delinsTA | |
NM_000769.4:c.819+216_819+217delinsTA MANE Select | NP_000760.1:n.819+216_819+217delinsTA |