HGVS | Genome Assembly |
---|---|
NC_000014.9:g.23420149del , CM000676.2:g.23420149del | GRCh38 |
NC_000014.8:g.23889358del , CM000676.1:g.23889358del | GRCh37 |
NC_000014.7:g.22959198del | NCBI36 |
NG_007884.1:g.20515del , LRG_384:g.20515del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000355349.4:c.3424del MANE Select | ENSP00000347507.3:p.Glu1142SerfsTer22 | |
ENST00000355349.3:c.3424del | ENSP00000347507.3:p.Glu1142SerfsTer22 | |
NM_000257.3:c.3424del | NP_000248.2:p.Glu1142SerfsTer22 | |
XM_017021340.1:c.3424del | XP_016876829.1:p.Glu1142SerfsTer22 | |
NM_000257.4:c.3424del MANE Select | NP_000248.2:p.Glu1142SerfsTer22 |