HGVS | Genome Assembly |
---|---|
NC_000004.12:g.88008204dup , CM000666.2:g.88008204dup | GRCh38 |
NC_000004.11:g.88929356dup , CM000666.1:g.88929356dup | GRCh37 |
NC_000004.10:g.89148380dup | NCBI36 |
NG_008604.1:g.5537dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000237596.7:c.471dup MANE Select | ENSP00000237596.2:p.Glu158ArgfsTer? | |
ENST00000237596.6:c.471dup | ENSP00000237596.2:p.Glu158ArgfsTer? | |
NM_000297.3:c.471dup | NP_000288.1:p.Glu158ArgfsTer? | |
XM_011532028.1:c.471dup | XP_011530330.1:p.Glu158ArgfsTer? | |
XR_244632.2:n.566dup | ||
NR_156488.1:n.558dup | ||
XM_011532028.2:c.471dup | XP_011530330.1:p.Glu158ArgfsTer? | |
NM_000297.4:c.471dup MANE Select | NP_000288.1:p.Glu158ArgfsTer? | |
NR_156488.2:n.570dup |