HGVS | Genome Assembly |
---|---|
NC_000020.11:g.33443527_33443529dup , CM000682.2:g.33443527_33443529dup | GRCh38 |
NC_000020.10:g.32031333_32031335dup , CM000682.1:g.32031333_32031335dup | GRCh37 |
NC_000020.9:g.31494994_31494996dup | NCBI36 |
NG_011622.1:g.5369_5371dup , LRG_332:g.5369_5371dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000217381.3:c.97_99dup MANE Select | ENSP00000217381.2:p.Leu33_Ser34insLeu | |
ENST00000217381.2:c.97_99dup | ENSP00000217381.2:p.Leu33_Ser34insLeu | |
NM_003098.2:c.97_99dup , LRG_332t1:c.97_99dup | NP_003089.1:p.Leu33_Ser34insLeu | |
XM_005260517.1:c.97_99dup | XP_005260574.1:p.Leu33_Ser34insLeu | |
XM_011529007.1:c.97_99dup | XP_011527309.1:p.Leu33_Ser34insLeu | |
XM_011529008.1:c.97_99dup | XP_011527310.1:p.Leu33_Ser34insLeu | |
XR_936612.1:n.330_332dup | ||
NM_003098.3:c.97_99dup MANE Select | NP_003089.1:p.Leu33_Ser34insLeu |