HGVS | Genome Assembly |
---|---|
NC_000017.11:g.34256171_34256172delinsGA , CM000679.2:g.34256171_34256172delinsGA | GRCh38 |
NC_000017.10:g.32583190_32583191delinsGA , CM000679.1:g.32583190_32583191delinsGA | GRCh37 |
NC_000017.9:g.29607303_29607304delinsGA | NCBI36 |
NG_012123.1:g.5895_5896delinsGA |
HGVS | Amino-acid change | |
---|---|---|
ENST00000580907.6:c.77-51_77-50delinsGA | ENSP00000462156.1:n.77-51_77-50delinsGA | |
ENST00000624362.2:n.887_888delinsGA | ||
ENST00000225831.4:c.77-51_77-50delinsGA MANE Select | ENSP00000225831.4:n.77-51_77-50delinsGA | |
ENST00000580907.5:c.77-51_77-50delinsGA | ENSP00000462156.1:n.77-51_77-50delinsGA | |
ENST00000624362.1:n.954_955delinsGA | ||
NM_002982.3:c.77-51_77-50delinsGA | NP_002973.1:n.77-51_77-50delinsGA | |
NM_002982.4:c.77-51_77-50delinsGA MANE Select | NP_002973.1:n.77-51_77-50delinsGA |