HGVS | Genome Assembly |
---|---|
NC_000007.14:g.141973274_141973275insCAATTTATTTTAT , CM000669.2:g.141973274_141973275insCAATTTATTTTAT | GRCh38 |
NC_000007.13:g.141673074_141673075insCAATTTATTTTAT , CM000669.1:g.141673074_141673075insCAATTTATTTTAT | GRCh37 |
NC_000007.12:g.141319543_141319544insCAATTTATTTTAT | NCBI36 |
NG_016141.1:g.5500_5501insTAAAATAAATTGA |
HGVS | Amino-acid change | |
---|---|---|
ENST00000465654.5:c.-3+27277_-3+27278insCAATTTATTTTAT (MGAM) | ENSP00000419372.1:n.-3+27277_-3+27278insC... | |
ENST00000547270.1:c.416_417insTAAAATAAATTGA (TAS2R38) MANE Select | ENSP00000448219.1:p.Lys139AsnfsTer5 | |
NM_176817.4:c.416_417insTAAAATAAATTGA (TAS2R38) | NP_789787.4:p.Lys139AsnfsTer5 | |
XM_011515783.1:c.*25-13122_*25-13121insCAATTTATTTTAT (OR9A4) | XP_011514085.1:n.*25-13122_*25-13121insCA... | |
NM_176817.5:c.416_417insTAAAATAAATTGA (TAS2R38) MANE Select | NP_789787.5:p.Lys139AsnfsTer5 |