HGVS | Genome Assembly |
---|---|
NC_000005.10:g.149981399_149981402del , CM000667.2:g.149981399_149981402del | GRCh38 |
NC_000005.9:g.149360962_149360965del , CM000667.1:g.149360962_149360965del | GRCh37 |
NC_000005.8:g.149341155_149341158del | NCBI36 |
NG_007147.2:g.22517_22520del , LRG_684:g.22517_22520del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000286298.5:c.1806_1809del MANE Select | ENSP00000286298.4:p.Thr603SerfsTer5 | |
ENST00000286298.4:c.1806_1809del | ENSP00000286298.4:p.Thr603SerfsTer5 | |
ENST00000503336.1:c.372+3048_372+3051del | ENSP00000426053.1:n.372+3048_372+3051del | |
NM_000112.3:c.1806_1809del , LRG_684t1:c.1806_1809del | NP_000103.2:p.Thr603SerfsTer5 | |
XM_017009191.2:c.1806_1809del | XP_016864680.1:p.Thr603SerfsTer5 | |
NM_000112.4:c.1806_1809del MANE Select | NP_000103.2:p.Thr603SerfsTer5 |