HGVS | Genome Assembly |
---|---|
NC_000021.9:g.45990464_45990466delinsGAA , CM000683.2:g.45990464_45990466delinsGAA | GRCh38 |
NC_000021.8:g.47410378_47410380delinsGAA , CM000683.1:g.47410378_47410380delinsGAA | GRCh37 |
NC_000021.7:g.46234806_46234808delinsGAA | NCBI36 |
NG_008674.1:g.13716_13718delinsGAA , LRG_475:g.13716_13718delinsGAA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000361866.8:c.1002+42_1002+44delinsGAA MANE Select | ENSP00000355180.3:n.1002+42_1002+44delinsGAA | |
ENST00000361866.7:c.1002+42_1002+44delinsGAA | ENSP00000355180.3:n.1002+42_1002+44delinsGAA | |
ENST00000612273.1:c.1002+42_1002+44delinsGAA | ENSP00000483630.1:n.1002+42_1002+44delinsGAA | |
NM_001848.2:c.1002+42_1002+44delinsGAA , LRG_475t1:c.1002+42_1002+44delinsGAA | NP_001839.2:n.1002+42_1002+44delinsGAA | |
NM_001848.3:c.1002+42_1002+44delinsGAA MANE Select | NP_001839.2:n.1002+42_1002+44delinsGAA |