HGVS | Genome Assembly |
---|---|
NC_000010.11:g.94780695_94780697delinsTAC , CM000672.2:g.94780695_94780697delinsTAC | GRCh38 |
NC_000010.10:g.96540452_96540454delinsTAC , CM000672.1:g.96540452_96540454delinsTAC | GRCh37 |
NC_000010.9:g.96530442_96530444delinsTAC | NCBI36 |
NG_008384.2:g.22990_22992delinsTAC | |
NG_008384.3:g.23015_23017delinsTAC |
HGVS | Amino-acid change | |
---|---|---|
ENST00000371321.9:c.642+36_642+38delinsTAC MANE Select | ENSP00000360372.3:n.642+36_642+38delinsTA... | |
ENST00000645461.1:n.1695+36_1695+38delinsTAC | ||
ENST00000371321.7:c.642+36_642+38delinsTAC | ENSP00000360372.3:n.642+36_642+38delinsTA... | |
ENST00000464755.1:c.1405+36_1405+38delinsTAC | ENSP00000483243.1:n.1405+36_1405+38delins... | |
NM_000769.2:c.642+36_642+38delinsTAC | NP_000760.1:n.642+36_642+38delinsTAC | |
NM_000769.4:c.642+36_642+38delinsTAC MANE Select | NP_000760.1:n.642+36_642+38delinsTAC |