HGVS | Genome Assembly |
---|---|
NC_000006.12:g.31125806_31125807insCGACC , CM000668.2:g.31125806_31125807insCGACC | GRCh38 |
NC_000006.11:g.31093583_31093584insCGACC , CM000668.1:g.31093583_31093584insCGACC | GRCh37 |
NC_000006.10:g.31201562_31201563insCGACC | NCBI36 |
NG_021348.1:g.15976_15977insCGACC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000259881.10:c.-98_-97insCGACC MANE Select | ENSP00000259881.9:n.-98_-97insCGACC | |
ENST00000259881.9:c.-98_-97insCGACC | ENSP00000259881.9:n.-98_-97insCGACC | |
ENST00000479581.5:n.61+10915_61+10916insCGACC | ||
ENST00000548049.1:n.247_248insCGACC | ||
ENST00000550838.1:n.126_127insCGACC | ||
ENST00000552747.1:n.53+10915_53+10916insCGACC | ||
NM_014068.2:c.-98_-97insCGACC | NP_054787.2:n.-98_-97insCGACC | |
NM_014068.3:c.-98_-97insCGACC MANE Select | NP_054787.2:n.-98_-97insCGACC |