HGVS | Genome Assembly |
---|---|
NC_000009.12:g.129813699_129813700delinsTA , CM000671.2:g.129813699_129813700delinsTA | GRCh38 |
NC_000009.11:g.132575978_132575979delinsTA , CM000671.1:g.132575978_132575979delinsTA | GRCh37 |
NC_000009.10:g.131615799_131615800delinsTA | NCBI36 |
NG_008049.1:g.15463_15464delinsTA |
HGVS | Amino-acid change | |
---|---|---|
ENST00000351698.5:c.*272_*273delinsTA MANE Select | ENSP00000345719.4:n.*272_*273delinsTA | |
ENST00000651202.1:c.*539_*540delinsTA | ENSP00000498222.1:n.*539_*540delinsTA | |
ENST00000351698.4:c.*272_*273delinsTA | ENSP00000345719.4:n.*272_*273delinsTA | |
ENST00000474192.1:n.855_856delinsTA | ||
NM_000113.2:c.*272_*273delinsTA | NP_000104.1:n.*272_*273delinsTA | |
XR_929731.3:n.1466_1467delinsTA | ||
NM_000113.3:c.*272_*273delinsTA MANE Select | NP_000104.1:n.*272_*273delinsTA |