HGVS | Genome Assembly |
---|---|
NC_000010.11:g.104034330del , CM000672.2:g.104034330del | GRCh38 |
NC_000010.10:g.105794088del , CM000672.1:g.105794088del | GRCh37 |
NC_000010.9:g.105784078del | NCBI36 |
NG_007069.1:g.56551del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000369733.8:c.3525del | ENSP00000358748.3:p.Asp1176MetfsTer? | |
ENST00000648076.2:c.3771del MANE Select | ENSP00000497653.1:p.Asp1258MetfsTer? | |
ENST00000353479.9:c.3771del | ENSP00000340937.5:p.Asp1258MetfsTer? | |
ENST00000369733.7:c.3525del | ENSP00000358748.3:p.Asp1176MetfsTer? | |
NM_000494.3:c.3771del | NP_000485.3:p.Asp1258MetfsTer? | |
NM_000494.4:c.3771del MANE Select | NP_000485.3:p.Asp1258MetfsTer? |