HGVS | Genome Assembly |
---|---|
NC_000001.11:g.154571694_154571695insA , CM000663.2:g.154571694_154571695insA | GRCh38 |
NC_000001.10:g.154544170_154544171insA , CM000663.1:g.154544170_154544171insA | GRCh37 |
NC_000001.9:g.152810794_152810795insA | NCBI36 |
NG_008027.1:g.8914_8915insA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000368476.4:c.871_872insA MANE Select | ENSP00000357461.3:p.Ser291TyrfsTer? | |
ENST00000636034.1:c.871_872insA | ENSP00000489703.1:p.Ser291TyrfsTer? | |
ENST00000637900.1:c.877_878insA | ENSP00000490474.1:p.Ser293TyrfsTer? | |
ENST00000368476.3:c.871_872insA | ENSP00000357461.3:p.Ser291TyrfsTer? | |
NM_000748.2:c.871_872insA | NP_000739.1:p.Ser291TyrfsTer? | |
XM_017000180.2:c.361_362insA | XP_016855669.1:p.Ser121TyrfsTer? | |
XR_001736952.2:n.1123_1124insA | ||
NM_000748.3:c.871_872insA MANE Select | NP_000739.1:p.Ser291TyrfsTer? |