HGVS | Genome Assembly |
---|---|
NC_000008.11:g.38145151_38145152delinsTG , CM000670.2:g.38145151_38145152delinsTG | GRCh38 |
NC_000008.10:g.38002669_38002670delinsTG , CM000670.1:g.38002669_38002670delinsTG | GRCh37 |
NC_000008.9:g.38121826_38121827delinsTG | NCBI36 |
NG_011827.1:g.10931_10932delinsCA |
HGVS | Amino-acid change | |
---|---|---|
ENST00000276449.9:c.744+70_744+71delinsCA MANE Select | ENSP00000276449.3:n.744+70_744+71delinsCA | |
ENST00000276449.8:c.744+70_744+71delinsCA | ENSP00000276449.3:n.744+70_744+71delinsCA | |
ENST00000520114.1:n.1948_1949delinsCA | ||
ENST00000522050.1:c.587-766_587-765delinsCA | ||
NM_000349.2:c.744+70_744+71delinsCA | NP_000340.2:n.744+70_744+71delinsCA | |
XM_006716392.1:c.651-766_651-765delinsCA | XP_006716455.1:n.651-766_651-765delinsCA | |
NM_000349.3:c.744+70_744+71delinsCA MANE Select | NP_000340.2:n.744+70_744+71delinsCA |