HGVS | Genome Assembly |
---|---|
NC_000009.12:g.134843194_134843196del , CM000671.2:g.134843194_134843196del | GRCh38 |
NC_000009.11:g.137735040_137735042del , CM000671.1:g.137735040_137735042del | GRCh37 |
NC_000009.10:g.136874861_136874863del | NCBI36 |
NG_008030.1:g.206389_206391del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000371820.4:c.*891_*893del | ENSP00000360885.4:n.*891_*893del | |
ENST00000371817.8:c.*891_*893del MANE Select | ENSP00000360882.3:n.*891_*893del | |
ENST00000371817.7:c.*891_*893del | ENSP00000360882.3:n.*891_*893del | |
ENST00000618395.4:c.*891_*893del | ENSP00000481360.1:n.*891_*893del | |
NM_000093.4:c.*891_*893del | NP_000084.3:n.*891_*893del | |
NM_001278074.1:c.*891_*893del | NP_001265003.1:n.*891_*893del | |
NR_103451.2:n.71-22985_71-22983del | ||
NM_000093.5:c.*891_*893del MANE Select | NP_000084.3:n.*891_*893del |