HGVS | Genome Assembly |
---|---|
NC_000002.12:g.202377459_202377460insG , CM000664.2:g.202377459_202377460insG | GRCh38 |
NC_000002.11:g.203242182_203242183insG , CM000664.1:g.203242182_203242183insG | GRCh37 |
NC_000002.10:g.202950427_202950428insG | NCBI36 |
NG_009363.1:g.6133_6134insG , LRG_712:g.6133_6134insG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000374580.10:c.-16_-15insG MANE Select | ENSP00000363708.4:n.-16_-15insG | |
ENST00000374574.2:c.-16_-15insG | ENSP00000363702.2:n.-16_-15insG | |
ENST00000374580.8:c.-16_-15insG | ENSP00000363708.4:n.-16_-15insG | |
NM_001204.6:c.-16_-15insG , LRG_712t1:c.-16_-15insG | NP_001195.2:n.-16_-15insG | |
XM_011511687.1:c.-16_-15insG | XP_011509989.1:n.-16_-15insG | |
XM_011511688.1:c.-16_-15insG | XP_011509990.1:n.-16_-15insG | |
NM_001204.7:c.-16_-15insG MANE Select | NP_001195.2:n.-16_-15insG |