HGVS | Genome Assembly |
---|---|
NC_000011.10:g.47333203_47333205del , CM000673.2:g.47333203_47333205del | GRCh38 |
NC_000011.9:g.47354754_47354756del , CM000673.1:g.47354754_47354756del | GRCh37 |
NC_000011.8:g.47311330_47311332del | NCBI36 |
NG_007667.1:g.24502_24504del , LRG_386:g.24502_24504del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000545968.6:c.3323_3325del MANE Select | ENSP00000442795.1:p.Lys1108del | |
ENST00000256993.8:c.3323_3325del | ENSP00000256993.5:p.Lys1108del | |
ENST00000399249.6:c.3323_3325del | ENSP00000382193.2:p.Lys1108del | |
ENST00000545968.5:c.3323_3325del | ENSP00000442795.1:p.Lys1108del | |
NM_000256.3:c.3323_3325del , LRG_386t1:c.3323_3325del MANE Select | NP_000247.2:p.Lys1108del | |
XM_011520117.1:c.3305_3307del | XP_011518419.1:p.Lys1102del | |
XM_011520118.1:c.3242_3244del | XP_011518420.1:p.Lys1081del |