HGVS | Genome Assembly |
---|---|
NC_000012.12:g.52492571_52492572insGTC , CM000674.2:g.52492571_52492572insGTC | GRCh38 |
NC_000012.11:g.52886355_52886356insGTC , CM000674.1:g.52886355_52886356insGTC | GRCh37 |
NC_000012.10:g.51172622_51172623insGTC | NCBI36 |
NG_008298.1:g.5826_5827insGAC |
HGVS | Amino-acid change | |
---|---|---|
ENST00000330722.7:c.540+77_540+78insGAC MANE Select | ENSP00000369317.3:n.540+77_540+78insGAC | |
ENST00000330722.6:c.540+77_540+78insGAC | ENSP00000369317.3:n.540+77_540+78insGAC | |
ENST00000549898.5:n.61+77_61+78insGAC | ||
NM_005554.3:c.540+77_540+78insGAC | NP_005545.1:n.540+77_540+78insGAC | |
NM_005554.4:c.540+77_540+78insGAC MANE Select | NP_005545.1:n.540+77_540+78insGAC |