HGVS | Genome Assembly |
---|---|
NC_000005.10:g.44305284_44305285delinsTC , CM000667.2:g.44305284_44305285delinsTC | GRCh38 |
NC_000005.9:g.44305386_44305387delinsTC , CM000667.1:g.44305386_44305387delinsTC | GRCh37 |
NC_000005.8:g.44341143_44341144delinsTC | NCBI36 |
NG_011446.1:g.88398_88399delinsGA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264664.5:c.430-93_430-92delinsGA MANE Select | ENSP00000264664.4:n.430-93_430-92delinsGA | |
ENST00000264664.4:c.430-93_430-92delinsGA | ENSP00000264664.4:n.430-93_430-92delinsGA | |
NM_004465.1:c.430-93_430-92delinsGA | NP_004456.1:n.430-93_430-92delinsGA | |
XM_005248264.2:c.430-93_430-92delinsGA | XP_005248321.1:n.430-93_430-92delinsGA | |
XM_005248264.4:c.430-93_430-92delinsGA | XP_005248321.1:n.430-93_430-92delinsGA | |
NM_004465.2:c.430-93_430-92delinsGA MANE Select | NP_004456.1:n.430-93_430-92delinsGA |