HGVS | Genome Assembly |
---|---|
NC_000023.11:g.154954051_154954052insG , CM000685.2:g.154954051_154954052insG | GRCh38 |
NC_000023.10:g.154182326_154182327insG , CM000685.1:g.154182326_154182327insG | GRCh37 |
NC_000023.9:g.153835520_153835521insG | NCBI36 |
NG_011403.1:g.73672_73673insC | |
NG_011403.2:g.73672_73673insC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000360256.9:c.1753-10_1753-9insC MANE Select | ENSP00000353393.4:n.1753-10_1753-9insC | |
ENST00000647125.1:c.*1629-10_*1629-9insC | ENSP00000496062.1:n.*1629-10_*1629-9insC | |
ENST00000360256.8:c.1753-10_1753-9insC | ENSP00000353393.4:n.1753-10_1753-9insC | |
NM_000132.3:c.1753-10_1753-9insC | NP_000123.1:n.1753-10_1753-9insC | |
XM_011531126.1:c.1648-10_1648-9insC | XP_011529428.1:n.1648-10_1648-9insC | |
NM_000132.4:c.1753-10_1753-9insC MANE Select | NP_000123.1:n.1753-10_1753-9insC |