HGVS | Genome Assembly |
---|---|
NC_000007.14:g.19116836del , CM000669.2:g.19116836del | GRCh38 |
NC_000007.13:g.19156459del , CM000669.1:g.19156459del | GRCh37 |
NC_000007.12:g.19122984del | NCBI36 |
NG_008114.1:g.5838del | |
NG_008114.2:g.5838del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000242261.6:c.487del MANE Select | ENSP00000242261.5:p.Leu163SerfsTer? | |
ENST00000242261.5:c.487del | ENSP00000242261.5:p.Leu163SerfsTer? | |
ENST00000354571.5:c.284del | ||
ENST00000443687.5:c.90del | ||
NM_000474.3:c.487del | NP_000465.1:p.Leu163SerfsTer? | |
XM_011515496.1:c.487del | XP_011513798.1:p.Leu163SerfsTer? | |
NR_149001.1:n.838del | ||
NM_000474.4:c.487del MANE Select | NP_000465.1:p.Leu163SerfsTer? | |
NR_149001.2:n.802del |