HGVS | Genome Assembly |
---|---|
NC_000010.11:g.94780696_94780697insTT , CM000672.2:g.94780696_94780697insTT | GRCh38 |
NC_000010.10:g.96540453_96540454insTT , CM000672.1:g.96540453_96540454insTT | GRCh37 |
NC_000010.9:g.96530443_96530444insTT | NCBI36 |
NG_008384.2:g.22991_22992insTT | |
NG_008384.3:g.23016_23017insTT |
HGVS | Amino-acid change | |
---|---|---|
ENST00000371321.9:c.642+37_642+38insTT MANE Select | ENSP00000360372.3:n.642+37_642+38insTT | |
ENST00000645461.1:n.1695+37_1695+38insTT | ||
ENST00000371321.7:c.642+37_642+38insTT | ENSP00000360372.3:n.642+37_642+38insTT | |
ENST00000464755.1:c.1405+37_1405+38insTT | ENSP00000483243.1:n.1405+37_1405+38insTT | |
NM_000769.2:c.642+37_642+38insTT | NP_000760.1:n.642+37_642+38insTT | |
NM_000769.4:c.642+37_642+38insTT MANE Select | NP_000760.1:n.642+37_642+38insTT |