HGVS | Genome Assembly |
---|---|
NC_000004.12:g.88007798_88007799delinsTT , CM000666.2:g.88007798_88007799delinsTT | GRCh38 |
NC_000004.11:g.88928950_88928951delinsTT , CM000666.1:g.88928950_88928951delinsTT | GRCh37 |
NC_000004.10:g.89147974_89147975delinsTT | NCBI36 |
NG_008604.1:g.5131_5132delinsTT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000237596.7:c.65_66delinsTT MANE Select | ENSP00000237596.2:p.Arg22Leu | |
ENST00000237596.6:c.65_66delinsTT | ENSP00000237596.2:p.Arg22Leu | |
NM_000297.3:c.65_66delinsTT | NP_000288.1:p.Arg22Leu | |
XM_011532028.1:c.65_66delinsTT | XP_011530330.1:p.Arg22Leu | |
XR_244632.2:n.160_161delinsTT | ||
NR_156488.1:n.152_153delinsTT | ||
XM_011532028.2:c.65_66delinsTT | XP_011530330.1:p.Arg22Leu | |
NM_000297.4:c.65_66delinsTT MANE Select | NP_000288.1:p.Arg22Leu | |
NR_156488.2:n.164_165delinsTT |