HGVS | Genome Assembly |
---|---|
NC_000002.12:g.29070732_29070749del , CM000664.2:g.29070732_29070749del | GRCh38 |
NC_000002.11:g.29293598_29293615del , CM000664.1:g.29293598_29293615del | GRCh37 |
NC_000002.10:g.29147102_29147119del | NCBI36 |
NG_021427.1:g.8521_8538del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000331664.6:c.3521_3538del MANE Select | ENSP00000332809.4:p.Asp1174_Ala1179del | |
ENST00000331664.5:c.3521_3538del | ENSP00000332809.4:p.Asp1174_Ala1179del | |
NM_001029883.2:c.3521_3538del | NP_001025054.1:p.Asp1174_Ala1179del | |
XM_011532826.1:c.3521_3538del | XP_011531128.1:p.Asp1174_Ala1179del | |
XR_939901.1:n.185+1565_185+1582del | ||
XR_939902.1:n.173+1577_173+1594del | ||
NM_001029883.3:c.3521_3538del MANE Select | NP_001025054.1:p.Asp1174_Ala1179del |