HGVS | Genome Assembly |
---|---|
NC_000001.11:g.204190788_204190791del , CM000663.2:g.204190788_204190791del | GRCh38 |
NC_000001.10:g.204159916_204159919del , CM000663.1:g.204159916_204159919del | GRCh37 |
NC_000001.9:g.202426539_202426542del | NCBI36 |
NG_032151.1:g.10703_10706del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000367194.5:c.112_115del MANE Select | ENSP00000356162.4:p.Leu38AsnfsTer26 | |
ENST00000367194.4:c.112_115del | ENSP00000356162.4:p.Leu38AsnfsTer26 | |
ENST00000625357.1:c.112_115del | ENSP00000485957.1:p.Leu38AsnfsTer26 | |
NM_002256.3:c.112_115del | NP_002247.3:p.Leu38AsnfsTer26 | |
XM_011509525.1:c.112_115del | XP_011507827.1:p.Leu38AsnfsTer26 | |
NM_002256.4:c.112_115del MANE Select | NP_002247.3:p.Leu38AsnfsTer26 |