HGVS | Genome Assembly |
---|---|
NC_000005.10:g.149981398_149981401del , CM000667.2:g.149981398_149981401del | GRCh38 |
NC_000005.9:g.149360961_149360964del , CM000667.1:g.149360961_149360964del | GRCh37 |
NC_000005.8:g.149341154_149341157del | NCBI36 |
NG_007147.2:g.22516_22519del , LRG_684:g.22516_22519del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000286298.5:c.1805_1808del MANE Select | ENSP00000286298.4:p.Gln602LeufsTer6 | |
ENST00000286298.4:c.1805_1808del | ENSP00000286298.4:p.Gln602LeufsTer6 | |
ENST00000503336.1:c.372+3047_372+3050del | ENSP00000426053.1:n.372+3047_372+3050del | |
NM_000112.3:c.1805_1808del , LRG_684t1:c.1805_1808del | NP_000103.2:p.Gln602LeufsTer6 | |
XM_017009191.2:c.1805_1808del | XP_016864680.1:p.Gln602LeufsTer6 | |
NM_000112.4:c.1805_1808del MANE Select | NP_000103.2:p.Gln602LeufsTer6 |