HGVS | Genome Assembly |
---|---|
NC_000004.12:g.186085386_186085387insAAGGA , CM000666.2:g.186085386_186085387insAAGGA | GRCh38 |
NC_000004.11:g.187006540_187006541insAAGGA , CM000666.1:g.187006540_187006541insAAGGA | GRCh37 |
NC_000004.10:g.187243534_187243535insAAGGA | NCBI36 |
NG_007278.1:g.21232_21233insAAGGA , LRG_117:g.21232_21233insAAGGA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000698352.1:c.*2780_*2781insAAGGA | ENSP00000513675.1:n.*2780_*2781insAAGGA | |
ENST00000698353.1:n.3103_3104insAAGGA | ||
ENST00000698354.1:c.*513_*514insAAGGA | ENSP00000513676.1:n.*513_*514insAAGGA | |
ENST00000296795.8:c.*513_*514insAAGGA MANE Select | ENSP00000296795.3:n.*513_*514insAAGGA | |
ENST00000296795.7:c.*513_*514insAAGGA | ENSP00000296795.2:n.*513_*514insAAGGA | |
NM_003265.3:c.*513_*514insAAGGA MANE Select | NP_003256.1:n.*513_*514insAAGGA |