HGVS | Genome Assembly |
---|---|
NC_000023.11:g.8731944_8731954del , CM000685.2:g.8731944_8731954del | GRCh38 |
NC_000023.10:g.8699985_8699995del , CM000685.1:g.8699985_8699995del | GRCh37 |
NC_000023.9:g.8659985_8659995del | NCBI36 |
NG_007088.1:g.5240_5250del | |
NG_007088.2:g.5240_5250del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000262648.8:c.90_100del MANE Select | ENSP00000262648.3:p.Ala32GlyfsTer? | |
ENST00000262648.7:c.90_100del | ENSP00000262648.3:p.Ala32GlyfsTer? | |
ENST00000619786.1:c.89_98del | ||
NM_000216.2:c.90_100del | NP_000207.2:p.Ala32GlyfsTer? | |
XM_005274501.3:c.90_100del | XP_005274558.1:p.Ala32GlyfsTer? | |
NM_000216.3:c.90_100del | NP_000207.2:p.Ala32GlyfsTer? | |
XM_005274501.4:c.90_100del | XP_005274558.1:p.Ala32GlyfsTer? | |
NM_000216.4:c.90_100del MANE Select | NP_000207.2:p.Ala32GlyfsTer? |