HGVS | Genome Assembly |
---|---|
NC_000009.12:g.38396348_38396349insAAACCG , CM000671.2:g.38396348_38396349insAAACCG | GRCh38 |
NC_000009.11:g.38396345_38396346insAAACCG , CM000671.1:g.38396345_38396346insAAACCG | GRCh37 |
NC_000009.10:g.38386345_38386346insAAACCG | NCBI36 |
NG_012253.1:g.8644_8645insAAACCG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000377698.4:c.600_601insAAACCG MANE Select | ENSP00000366927.3:p.Leu200_Ala201insLysPro | |
ENST00000377698.3:c.600_601insAAACCG | ENSP00000366927.3:p.Leu200_Ala201insLysPro | |
NM_000692.4:c.600_601insAAACCG | NP_000683.3:p.Leu200_Ala201insLysPro | |
XM_011517802.1:c.600_601insAAACCG | XP_011516104.1:p.Leu200_Ala201insLysPro | |
XM_011517802.2:c.600_601insAAACCG | XP_011516104.1:p.Leu200_Ala201insLysPro | |
NM_000692.5:c.600_601insAAACCG MANE Select | NP_000683.3:p.Leu200_Ala201insLysPro |