HGVS | Genome Assembly |
---|---|
NC_000007.14:g.94401528_94401529insA , CM000669.2:g.94401528_94401529insA | GRCh38 |
NC_000007.13:g.94030840_94030841insA , CM000669.1:g.94030840_94030841insA | GRCh37 |
NC_000007.12:g.93868776_93868777insA | NCBI36 |
NG_007405.1:g.11968_11969insA , LRG_2:g.11968_11969insA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000297268.11:c.226-39_226-38insA MANE Select | ENSP00000297268.6:n.226-39_226-38insA | |
ENST00000297268.10:c.226-39_226-38insA | ENSP00000297268.6:n.226-39_226-38insA | |
ENST00000620463.1:c.220-39_220-38insA | ENSP00000477719.1:n.220-39_220-38insA | |
NM_000089.3:c.226-39_226-38insA , LRG_2t1:c.226-39_226-38insA | NP_000080.2:n.226-39_226-38insA | |
NM_000089.4:c.226-39_226-38insA MANE Select | NP_000080.2:n.226-39_226-38insA |